Atlas FDA

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

LEA — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K873594TIF FECAL TESTDevetec, Inc.1987-09-29250
K770592CYTOLOGY FIXATIVESurgipath Medical Industries, Inc.1977-05-20530
K761001PAP-TRAY II (CATALOG #C600-2)Lerner Laboratories, Inc.1976-12-06280
K761000PAP-TRAY I (CATALOG #C600-1)Lerner Laboratories, Inc.1976-12-06280

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