Clinical Connections, Inc.: FDA filings under this applicant name
FDA lists 10 510(k) clearances under the applicant name “Clinical Connections, Inc.” (first 1987, latest 1988), across 6 product codes in 3 review panels. Median 510(k) review time under this name: 29 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 |
|---|---|---|---|
| FPK | Tubing, Fluid Delivery | 3 | 3 |
| DTL | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | 2 | 2 |
| FMG | Stopcock, I.V. Set | 2 | 2 |
| FIB | Protector, Transducer, Dialysis | 1 | 1 |
| FPA | Set, Administration, Intravascular | 1 | 1 |
Plus 1 more product codes.
Review panels
Most recent Clinical Connections, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K884435 | RESUBMITTED 1,3 & 4 WAY STOPCOCKS, VARIOUS PARTS | FMG | 1988-11-08 | 26 |
| K871540 | SWIVEL CONNECTORS #014452/#014453/#014459-120 | FPK | 1987-04-30 | 23 |
| K870325 | #014160-TAB TUBING ROTATOR ADAPTOR | DTL | 1987-04-27 | 89 |
| K870477 | DEVICE CONNECTORS #000299-000 3/8 X 3/8 X 3/8 Y | — | 1987-04-03 | 59 |
| K870913 | INJECTION SITE #014456-120 | FPA | 1987-03-17 | 11 |
| K870912 | T-CONNECTORS 014500/014501/014502/014503-120 | FPK | 1987-03-17 | 11 |
| K870324 | #014460-120 3-WAY & #014461-120 4-WAY STOPCOCK | FMG | 1987-03-13 | 44 |
| K870394 | HYDROPHOBIC #6194418/HYDRAPHILIC #6104418 FILTERS | FIB | 1987-03-03 | 32 |
| K870073 | MANIFOLD SWIVEL ROTATOR MODELS 014320 & 014321-TAB | DTL | 1987-02-20 | 43 |
| K870326 | VARIOUS LUER AND TUBING FITTINGS | FPK | 1987-02-10 | 13 |
Recalls
openFDA lists no recalls under a recalling firm named Clinical Connections, Inc..
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.
- Clinical Data, Inc. (37 510(k)s)
- Clinical Sciences, Inc. (30 510(k)s)
- Clinical Assays, Inc. (27 510(k)s)
- Clinical Controls, Inc. (18 510(k)s)
- Clinical Innovations, LLC (18 510(k)s)
- Clinical Resources, Inc. (14 510(k)s)
- Clinical Technology Corp. (12 510(k)s)
- Clinical Diagnostics, Inc. (8 510(k)s)
- Clinical Convenience Products, Inc. (6 510(k)s)
- Clinical Laserthermia Systems, AB (6 510(k)s)
- Clinical Neuro Systems, LLC (5 510(k)s)
- Clinical Bioresearch (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Clinical Connections, Inc.?
FDA lists 10 510(k) clearances under the applicant name “Clinical Connections, Inc.” (first 1987, latest 1988), across 6 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 Clinical Connections, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Clinical Connections, Inc. is 29 days.
Which FDA product codes appear under Clinical Connections, Inc.?
The most frequent FDA product codes under this applicant name are FPK (Tubing, Fluid Delivery, 3); DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass, 2); FMG (Stopcock, I.V. Set, 2).
Next steps
- See all 10 Clinical Connections, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FPK, Clinical Connections, Inc.'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.