Berman, Pcp & Consultants, Inc.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Berman, Pcp & Consultants, Inc.” (first 1977, latest 1978), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 84 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | 5 | 5 |
| FMF | Syringe, Piston | 1 | 1 |
| FPK | Tubing, Fluid Delivery | 1 | 1 |
Review panels
- General Hospital (7)
Most recent Berman, Pcp & Consultants, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K771983 | SCALP VEIN SET | FPA | 1978-01-05 | 79 |
| K771272 | DISP. SYRINGES: 2,5 & L0 MI. | FMF | 1977-09-12 | 84 |
| K771271 | SCALP VEIN SET | FPA | 1977-09-12 | 84 |
| K771270 | BLOOD ADMINISTRATION TYPE R | FPA | 1977-09-12 | 84 |
| K771269 | BLOOD COLLECTION SET TYPE H | FPK | 1977-09-12 | 84 |
| K771268 | INFUSION SET TYPE J | FPA | 1977-09-12 | 84 |
| K771267 | INFUSION SET TYPE S | FPA | 1977-09-12 | 84 |
Recalls
openFDA lists no recalls under a recalling firm named Berman, Pcp & Consultants, 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Berman, Pcp & Consultants, Inc.?
FDA lists 7 510(k) clearances under the applicant name “Berman, Pcp & Consultants, Inc.” (first 1977, latest 1978), across 3 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Berman, Pcp & Consultants, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Berman, Pcp & Consultants, Inc. is 84 days.
Which FDA product codes appear under Berman, Pcp & Consultants, Inc.?
The most frequent FDA product codes under this applicant name are FPA (Set, Administration, Intravascular, 5); FMF (Syringe, Piston, 1); FPK (Tubing, Fluid Delivery, 1).
Next steps
- See all 7 Berman, Pcp & Consultants, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FPA, Berman, Pcp & Consultants, 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.