Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Medical Products Search, Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K905665PATIENT EXAMINATION GLOVESMedical Products Search, Inc.1991-01-15280
K885324HEMA(PRO)TEC(TION)Medical Products Search, Inc.1989-02-17510
K874454IV-PUSH, CONSTANT INFUSION PUMPMedical Products Search, Inc.1987-11-0690

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