Vee Gee Scientific, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Vee Gee Scientific, Inc.” (first 1994, latest 1995), across 1 product code in 1 review panel. Median 510(k) review time under this name: 256 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 |
|---|---|---|---|
| JRE | Refractometer For Clinical Use | 6 | 6 |
Review panels
Most recent Vee Gee Scientific, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K941906 | MODEL 2730 CLINICAL REFRACTOMETER | JRE | 1995-01-17 | 273 |
| K941903 | MODEL 2740 CLINICAL REFRACTOMETER | JRE | 1995-01-17 | 273 |
| K941901 | MODEL 2721 CLINICAL REFRACTOMETER | JRE | 1995-01-17 | 273 |
| K941905 | MODEL 3461 CLINICAL REFRACTOMETER | JRE | 1994-12-13 | 238 |
| K941904 | MODEL A300CL CLINICAL REFRACTOMETER | JRE | 1994-12-13 | 238 |
| K941902 | MODEL 3471 CLINICAL REFRACTOMETER | JRE | 1994-12-13 | 238 |
Recalls
openFDA lists no recalls under a recalling firm named Vee Gee Scientific, 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 Vee Gee Scientific, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Vee Gee Scientific, Inc.” (first 1994, latest 1995), across 1 product code 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 Vee Gee Scientific, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Vee Gee Scientific, Inc. is 256 days.
Which FDA product codes appear under Vee Gee Scientific, Inc.?
The most frequent FDA product codes under this applicant name are JRE (Refractometer For Clinical Use, 6).
Next steps
- See all 6 Vee Gee Scientific, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JRE, Vee Gee Scientific, 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.