Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medicorp, Inc. — Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
101 daysmedian FDA review time
318 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K860026 | ULTRAMAX III, DIALYZER REPROCESSING DEVICE | Medicorp, Inc. | 1986-03-14 | 70 | 0 |
| K844850 | MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT | Medicorp, Inc. | 1985-04-02 | 110 | 0 |
| K832705 | ULTRAMAX | Medicorp, Inc. | 1984-06-25 | 318 | 0 |
| K791164 | NEGATOVE PRESSURE CONVERTOR | Medicorp, Inc. | 1979-10-04 | 101 | 0 |
| K791396 | MEDI-TRAK PORTABLE TRACTION DEVICE | Medicorp, Inc. | 1979-08-16 | 37 | 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