W.G. Whitney Corp.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “W.G. Whitney Corp.” (first 1977, latest 1984), across 7 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 |
|---|---|---|---|
| EFQ | Gauze/Sponge, Internal | 1 | 1 |
| FMH | Container, Specimen, Sterile | 1 | 1 |
| FRO | Dressing, Wound, Drug | 1 | 1 |
| IME | Pack, Hot Or Cold, Reusable | 1 | 1 |
| KDD | Kit, Surgical Instrument, Disposable | 1 | 1 |
| KGX | Tape And Bandage, Adhesive | 1 | 1 |
Plus 1 more product codes.
Review panels
Most recent W.G. Whitney Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K834532 | STERILE WET DRESSING PACK | KDD | 1984-01-25 | 35 |
| K813535 | XEROFORM DRESSING | FRO | 1982-02-04 | 49 |
| K810406 | STERILE WET DRESSING PACK | — | 1981-03-11 | 21 |
| K803299 | COLD/HOT PACK | IME | 1981-01-15 | 16 |
| K800907 | TOMAC WET DRESSING WARMER | KGX | 1980-05-20 | 29 |
| K781322 | STERILE WET DRESSING PACK | EFQ | 1978-08-17 | 17 |
| K770387 | UNICATCH | FMH | 1977-04-05 | 36 |
Recalls
openFDA lists no recalls under a recalling firm named W.G. Whitney Corp..
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 W.G. Whitney Corp.?
FDA lists 7 510(k) clearances under the applicant name “W.G. Whitney Corp.” (first 1977, latest 1984), across 7 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 W.G. Whitney Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name W.G. Whitney Corp. is 29 days.
Which FDA product codes appear under W.G. Whitney Corp.?
The most frequent FDA product codes under this applicant name are EFQ (Gauze/Sponge, Internal, 1); FMH (Container, Specimen, Sterile, 1); FRO (Dressing, Wound, Drug, 1).
Next steps
- See all 7 W.G. Whitney Corp. clearances with predicates and recalls
- Run predicate analysis for product code EFQ, W.G. Whitney Corp.'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.