Vee Gee Scientific, Inc.
Kirkland, WA, US
Vee Gee Scientific, Inc. appears in FDA device records in Kirkland, WA. FDA records list 6 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Vee Gee Scientific, Inc. between 1994 and 1995. The busiest year on record is 1994, with 3. The most recent is 1995, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 3 |
| 1995 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K941906 | MODEL 2730 CLINICAL REFRACTOMETER | JRE | Substantially Equivalent | |
| K941903 | MODEL 2740 CLINICAL REFRACTOMETER | JRE | Substantially Equivalent | |
| K941901 | MODEL 2721 CLINICAL REFRACTOMETER | JRE | Substantially Equivalent | |
| K941905 | MODEL 3461 CLINICAL REFRACTOMETER | JRE | Substantially Equivalent | |
| K941904 | MODEL A300CL CLINICAL REFRACTOMETER | JRE | Substantially Equivalent | |
| K941902 | MODEL 3471 CLINICAL REFRACTOMETER | JRE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain