Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Puracath Medical, Inc. — 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) |
|---|---|---|---|---|---|
| K251375 | PuraCath Firefly Needleless Connector IT (9005) | Puracath Medical, Inc. | 2026-02-12 | 286 | 0 |
| K203796 | Firefly Needleless Connector | Puracath Medical, Inc. | 2021-07-30 | 214 | 0 |
| K151620 | Firefly Peritoneal Dialysis Connector Disinfection System | Puracath Medical, Inc. | 2016-01-20 | 218 | 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