Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Hospital Products Co. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
20 daysmedian FDA review time
49 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K823696 | MICRO Z BLOOD COLLECTING NEEDLES | Hospital Products Co. | 1983-01-26 | 49 | 0 |
| K810318 | PARKE-DAVIS NON-WOVEN SPONGE | Hospital Products Co. | 1981-02-26 | 20 | 0 |
| K801602 | DESERET I.V. FILTER | Hospital Products Co. | 1980-08-27 | 44 | 0 |
| K801173 | ANGIO-FLO MONITORING KIT | Hospital Products Co. | 1980-05-28 | 12 | 0 |
| K792386 | NUTRA-PH INSTRUMENT MILK | Hospital Products Co. | 1979-12-10 | 14 | 0 |
| K791350 | POPE AMBULATORY HALO VEST | Hospital Products Co. | 1979-08-03 | 17 | 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