Atlas FDA

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

Laprol Scientific, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K831498URI-TEST 3, INLAB REAGENT STRIPS-URINALLaprol Scientific, Inc.1983-06-22420
K831499GLUCOSE 3, INLAB REAGENT STRIPS-URINALYLaprol Scientific, Inc.1983-06-17370
K822709URITEST 9, INLAB REAGENT STRIPS URINALYLaprol Scientific, Inc.1983-01-281430

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