Atlas FDA

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

Davis Lead Aprons, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K912326DAVIS LEAD APRON - VARIOUS CATALOGUE NUMBERSDavis Lead Aprons, Inc.1992-03-182990
K912327DAVIS LEAD APRON GONADAL SHIELD-VARIOUS CAT. NOS.Davis Lead Aprons, Inc.1992-03-182990
K912378DAVIS LEAD APRON/RADIOGRAPHIC VARIOUS CAT. NUMBERSDavis Lead Aprons, Inc.1992-03-182940

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