Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Andwin Scientific — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K983599 | SAFETEX CHLAMYDIA TRACHOMATIS SPECIMEN COLLECTION KIT | Andwin Scientific | 1998-12-11 | 58 | 0 |
| K983428 | SAFETEX CERVICAL SCRAPER (PLASTIC) | Andwin Scientific | 1998-11-16 | 48 | 0 |
| K964698 | SAFETEX COMBINATION BLOOD (ALCOHOL, ETHYL) / URINE COLLECTIO | Andwin Scientific | 1997-03-03 | 101 | 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