Atlas FDA

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

KMN · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K894788DMI SERIES 90 EXAMINATION TABLEM.D. Intl., Inc.1989-09-08420
K801936PAD, EXAMINING TABLEVolunteer Blind Industries, Inc.1980-08-27150
K761110BED TRAYFred Sammons, Inc.1976-12-02130

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