Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Centocor, 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) |
|---|---|---|---|---|---|
| K963803 | CENTOCOR CA 15-3 RIA MODEL NO. 800-033 | Centocor, Inc. | 1997-05-23 | 242 | 0 |
| K954997 | CENTOCOR AGGRESTAT, COLLAGEN REAGENT, CONTROL REAGENT | Centocor, Inc. | 1996-01-24 | 84 | 0 |
| K820499 | FITC ANTI-RABIES MONOCLONAL GLOBULIN | Centocor, Inc. | 1982-04-16 | 52 | 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