Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vee Gee Scientific, Inc. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
273 daysmedian FDA review time
273 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K941901 | MODEL 2721 CLINICAL REFRACTOMETER | Vee Gee Scientific, Inc. | 1995-01-17 | 273 | 0 |
| K941906 | MODEL 2730 CLINICAL REFRACTOMETER | Vee Gee Scientific, Inc. | 1995-01-17 | 273 | 0 |
| K941903 | MODEL 2740 CLINICAL REFRACTOMETER | Vee Gee Scientific, Inc. | 1995-01-17 | 273 | 0 |
| K941905 | MODEL 3461 CLINICAL REFRACTOMETER | Vee Gee Scientific, Inc. | 1994-12-13 | 238 | 0 |
| K941902 | MODEL 3471 CLINICAL REFRACTOMETER | Vee Gee Scientific, Inc. | 1994-12-13 | 238 | 0 |
| K941904 | MODEL A300CL CLINICAL REFRACTOMETER | Vee Gee Scientific, Inc. | 1994-12-13 | 238 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda