Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Automated Medical Products Corp. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K942910 | DEEPVISON | Automated Medical Products Corp. | 1995-07-21 | 395 | 0 |
| K942818 | DEEP SUTURE | Automated Medical Products Corp. | 1994-08-25 | 71 | 0 |
| K942002 | RETRACTOR | Automated Medical Products Corp. | 1994-05-17 | 22 | 0 |
| K940199 | DISSECTOR | Automated Medical Products Corp. | 1994-03-30 | 76 | 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