Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Post Medical, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
72 daysmedian FDA review time
579 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K990371 | DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950 | Post Medical, Inc. | 1999-04-21 | 72 | 0 |
| K972536 | SYRINGE NEEDLE REMOVER (S.N.R.) | Post Medical, Inc. | 1997-08-15 | 68 | 0 |
| K925086 | AUTOMATIC NEEDLE DISCONECT (A.N.D.) | Post Medical, Inc. | 1994-05-09 | 579 | 0 |
| K925816 | SHARPS CONTAINMENT SYSTEM | Post Medical, Inc. | 1994-04-29 | 528 | 0 |
| K830946 | MALE EXTERNAL CATHETER | Post Medical, Inc. | 1983-04-28 | 35 | 0 |
| K830947 | SYRINGE/NEEDLE DISPOS-BOX-CUTTER/CRIMPER | Post Medical, Inc. | 1983-04-12 | 19 | 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