Professional Medical Services: FDA filings under this applicant name
FDA lists 19 510(k) clearances under the applicant name “Professional Medical Services” (first 1983, latest 1992), across 13 product codes in 6 review panels. Median 510(k) review time under this name: 72 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| DQO | Catheter, Intravascular, Diagnostic | 3 | 3 |
| DRE | Dilator, Vessel, For Percutaneous Catheterization | 2 | 2 |
| FMF | Syringe, Piston | 2 | 2 |
| KKX | Drape, Surgical, Antimicrobial | 2 | 2 |
| MAV | Syringe, Balloon Inflation | 2 | 2 |
| DWS | Instruments, Surgical, Cardiovascular | 1 | 1 |
| DYB | Introducer, Catheter | 1 | 1 |
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | 1 | 1 |
| HIO | Sampler, Amniotic Fluid (Amniocentesis Tray) | 1 | 1 |
| HOZ | Sponge, Ophthalmic | 1 | 1 |
Plus 3 more product codes.
Review panels
- Cardiovascular (9)
- General Hospital (5)
- Obstetrics and Gynecology (1)
- Ophthalmic (1)
- Radiology (1)
- General and Plastic Surgery (1)
Most recent Professional Medical Services 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K913094 | DISPOSABLE SLIDE VALVE MANIFOLD | DQO | 1992-01-27 | 199 |
| K910378 | PRESSURE MONITORING EXTENSION LINE | DQO | 1991-04-22 | 83 |
| K904508 | CONDOR ANALOG INFLATION SYRINGE | MAV | 1991-04-02 | 180 |
| K904954 | CONDOR DIGITAL INFLATION SYRINGE | MAV | 1991-01-16 | 72 |
| K902606 | RADIOPAQUE RULER | KPR | 1990-09-27 | 107 |
| K884577 | PROCEDURE READY TRAYS | FOZ | 1989-08-01 | 273 |
| K890471 | PMS ANGIO DRAPE | KKX | 1989-02-27 | 27 |
| K884497 | CONTROL SYRINGE | FMF | 1988-12-12 | 48 |
| K872448 | BLOOD CONTAINMENT PACK | LRO | 1987-11-17 | 147 |
| K864555 | 3 RING ATTACHMENT | FMF | 1986-12-01 | 12 |
9 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Professional Medical Services.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Professional Medical Products, Inc. (9 510(k)s)
- Professional Instruments Co. (3 510(k)s)
- Professional Latex Sdn Bhd (3 510(k)s)
- Professional Positioners, Inc. (3 510(k)s)
- Professional Dental Mfg., Inc. (2 510(k)s)
- Professional Services For Surgeons, Ltd. (2 510(k)s)
- Professional Supplies, Inc. (2 510(k)s)
- Professional Tape Co., Inc. (2 510(k)s)
- Professional Technologies Corp. (2 510(k)s)
- Professional Catheter Corp. (1 510(k)s)
- Professional Dental Studios (1 510(k)s)
- Professional Dental Technologies Therapeutics, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Professional Medical Services?
FDA lists 19 510(k) clearances under the applicant name “Professional Medical Services” (first 1983, latest 1992), across 13 product codes in 6 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Professional Medical Services?
The median time from FDA receipt to decision across 510(k)s cleared under the name Professional Medical Services is 72 days.
Which FDA product codes appear under Professional Medical Services?
The most frequent FDA product codes under this applicant name are DQO (Catheter, Intravascular, Diagnostic, 3); DRE (Dilator, Vessel, For Percutaneous Catheterization, 2); FMF (Syringe, Piston, 2).
Next steps
- See all 19 Professional Medical Services clearances with predicates and recalls
- Run predicate analysis for product code DQO, Professional Medical Services's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.