Femmepharma Consumer Healthcare, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Femmepharma Consumer Healthcare, LLC - FDA 510(k) Cleared Devices
Recent clearances: Satisfaite
1
Total
1
Cleared
0
Denied
Femmepharma Consumer Healthcare, LLC has 1 FDA 510(k) cleared medical devices. Based in Wayne, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Femmepharma Consumer Healthcare, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo by UL as regulatory consultant.
FDA 510(k) Regulatory Record - Femmepharma Consumer Healthcare, LLC
1 devices