Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Biowy Corporation · 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) |
|---|---|---|---|---|---|
| K233658 | Biowy Tym Tube (TT) | Biowy Corporation | 2024-02-16 | 93 | 0 |
| K192246 | Biowy PICC Catheter S Kit | Biowy Corporation | 2020-04-30 | 255 | 0 |
| K173956 | Biowy PlCC Catheter | Biowy Corporation | 2018-05-21 | 144 | 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