Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Professional Medical Products, Inc. · Predicate Candidate Screening
9 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
63 daysmedian FDA review time
735 days90th percentile
9clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K926280 | STANDARD NEBULIZER HEATER | Professional Medical Products, Inc. | 1994-03-22 | 463 | 0 |
| K930270 | PATIENT PREOPERATIVE PREP TRAY, SINGLE USE | Professional Medical Products, Inc. | 1994-02-17 | 394 | 0 |
| K920292 | VARIOUS KITS AND TRAYS | Professional Medical Products, Inc. | 1994-01-26 | 735 | 0 |
| K862010 | CHICK SURGICAL LIGHT | Professional Medical Products, Inc. | 1986-06-09 | 12 | 0 |
| K860739 | CHICK SURIGICAL LIGHT | Professional Medical Products, Inc. | 1986-03-28 | 29 | 0 |
| K834478 | CHICK/REISON PATIENT EMERG. TROLLEY | Professional Medical Products, Inc. | 1984-02-21 | 63 | 0 |
| K830825 | YIELD NON-ADHERENT DRESSING | Professional Medical Products, Inc. | 1983-05-13 | 59 | 0 |
| K822713 | DERM-A-TEC SKIN BARRIER FILM | Professional Medical Products, Inc. | 1982-12-07 | 91 | 0 |
| K820413 | AEGIS NON-ADHERENT DRESSING | Professional Medical Products, Inc. | 1982-03-12 | 28 | 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