Hancock Laboratories, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Hancock Laboratories, Inc.” (first 1978, latest 1980), across 5 product codes in 1 review panel. Median 510(k) review time under this name: 14 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 | 1 | 1 |
| DTI | Sizer, Heart-Valve, Prosthesis | 1 | 1 |
| DWS | Instruments, Surgical, Cardiovascular | 1 | 1 |
| KRH | Ring, Annuloplasty | 1 | 1 |
Plus 1 more product codes.
Review panels
- Cardiovascular (4)
Most recent Hancock Laboratories, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K801885 | HANCOCK * OBTURATORS | DTI | 1980-09-09 | 33 |
| K800703 | MODIFIED CATHETER PACKAGE | DQO | 1980-04-08 | 12 |
| K800122 | HANCOCK AORTIC PUNCH | DWS | 1980-02-01 | 14 |
| K790534 | MERSILENE SUTURES | KRH | 1979-03-26 | 13 |
| K780568 | DURAN FLEXIBLE RING | — | 1978-05-26 | 46 |
Recalls
openFDA lists no recalls under a recalling firm named Hancock Laboratories, 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.
- Hancock/Jaffe Laboratories (1 510(k)s)
- Hancock Medical, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Hancock Laboratories, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Hancock Laboratories, Inc.” (first 1978, latest 1980), across 5 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 Hancock Laboratories, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Hancock Laboratories, Inc. is 14 days.
Which FDA product codes appear under Hancock Laboratories, Inc.?
The most frequent FDA product codes under this applicant name are DQO (Catheter, Intravascular, Diagnostic, 1); DTI (Sizer, Heart-Valve, Prosthesis, 1); DWS (Instruments, Surgical, Cardiovascular, 1).
Next steps
- See all 5 Hancock Laboratories, Inc. clearances with predicates and recalls
- Run predicate analysis for product code DQO, Hancock Laboratories, 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 (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.