Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medpro, Inc. — 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) |
|---|---|---|---|---|---|
| K772062 | NEONATAL FLOTATION SYSTEM | Medpro, Inc. | 1977-11-15 | 13 | 0 |
| K771824 | MEDPRO FLOTATION SYSTEM | Medpro, Inc. | 1977-10-19 | 22 | 0 |
| K760870 | HEEL/ELBOW FLOTATION CUSHION | Medpro, Inc. | 1976-11-01 | 14 | 0 |
| K760613 | FLOTATION UNIT, CHAIR | Medpro, Inc. | 1976-10-14 | 34 | 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