Les Laboratoires Brothier S.A. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Les Laboratoires Brothier S.A. - FDA 510(k) Cleared Devices
Recent clearances: NasalCEASE and BleedCEASE
1
Total
1
Cleared
0
Denied
Les Laboratoires Brothier S.A. has 1 FDA 510(k) cleared medical devices. Based in Nanterre, FR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Les Laboratoires Brothier S.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Les Laboratoires Brothier S.A.
1 devices