Medical Marketing Group: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Medical Marketing Group” (first 1979, latest 1991), across 8 product codes in 3 review panels. Median 510(k) review time under this name: 35 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 |
|---|---|---|---|
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 4 | 4 |
| BYX | Tubing, Pressure And Accessories | 1 | 1 |
| BYZ | Trap, Sterile Specimen | 1 | 1 |
| FCM | Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit) | 1 | 1 |
| GAZ | Tubing, Noninvasive | 1 | 1 |
| GBM | Catheter, Urethral | 1 | 1 |
| KNY | Accessories, Catheter, G-U | 1 | 1 |
| KOD | Catheter, Urological | 1 | 1 |
Review panels
Most recent Medical Marketing Group 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K910022 | MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT | FCM | 1991-04-02 | 89 |
| K884819 | O'NEIL URINARY CATHETER INTRODUCER | KNY | 1989-02-17 | 92 |
| K874682 | MMG CATHETER PLUG W/DRAINAGE TUBE COVER | KOD | 1988-01-27 | 75 |
| K871999 | MMG URO-SELF CATHETER | GBM | 1987-08-25 | 91 |
| K863912 | THE MMG 5 IN 1 CONNECTOR | BYX | 1986-10-27 | 19 |
| K840838 | MMG CONNECTIVE TUBING | GAZ | 1984-03-30 | 35 |
| K821168 | DISPOSABLE URINARY LEGBAG W/STRAP | KNX | 1982-05-24 | 27 |
| K811469 | MMG URINARY DRAINAGE TUBING | KNX | 1981-06-12 | 17 |
| K800694 | MMG DISPOSABLE URINARY LEG BAG | KNX | 1980-05-30 | 64 |
| K791847 | ASPRI-LUKE | BYZ | 1979-10-02 | 13 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Medical Marketing Group.
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.
- Medical Analysis Systems, Inc. (107 510(k)s)
- Medical Components, Inc. (63 510(k)s)
- Medical Advances, Inc. (57 510(k)s)
- Medical Diagnostic Technologies, Inc. (57 510(k)s)
- Medical Devices, Inc. (49 510(k)s)
- Medical Device Technologies, Inc. (46 510(k)s)
- Medical Specialties, Inc. (40 510(k)s)
- Medical Device Inspection Co., Inc. (30 510(k)s)
- Medical Engineering Corp. (28 510(k)s)
- Medical Data Electronics (27 510(k)s)
- Medical Graphics Corp. (25 510(k)s)
- Medical Innovations Corp. (24 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Medical Marketing Group?
FDA lists 11 510(k) clearances under the applicant name “Medical Marketing Group” (first 1979, latest 1991), across 8 product codes in 3 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 Medical Marketing Group?
The median time from FDA receipt to decision across 510(k)s cleared under the name Medical Marketing Group is 35 days.
Which FDA product codes appear under Medical Marketing Group?
The most frequent FDA product codes under this applicant name are KNX (Collector, Urine, (And Accessories) For Indwelling Catheter, 4); BYX (Tubing, Pressure And Accessories, 1); BYZ (Trap, Sterile Specimen, 1).
Next steps
- See all 11 Medical Marketing Group clearances with predicates and recalls
- Run predicate analysis for product code KNX, Medical Marketing Group'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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.