FDA applicant
Laprol Scientific, Inc.
FDA records 3 decisions for Laprol Scientific, Inc. (Mchenry, IL) in 1983: 3 510(k) clearances. Most are in product codes JIL (Method, Enzymatic, Glucose (Urinary…) and JMA (Acid, Ascorbic, 2,4-Dinitrophenylhydrazine…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Laprol Scientific, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Laprol Scientific, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Laprol Scientific, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report