Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Medical Profiles, Inc. — Predicate Candidate Screening

3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K914378PERIPHERAL INTERVENOUS CATHETERMedical Profiles, Inc.1993-05-205970
K884327EXCEL Y-CONNECTOR CAT. #E-201Medical Profiles, Inc.1989-04-191870
K883769EXCEL INFLATE-AIDMedical Profiles, Inc.1988-12-01860

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