Peptonic Medical AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Peptonic Medical AB - FDA 510(k) Cleared Devices
Recent clearances: VagiVital Aktivgel
1
Total
1
Cleared
0
Denied
Peptonic Medical AB has 1 FDA 510(k) cleared medical devices. Based in Bromma, SE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Peptonic Medical AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by J&D Campbell Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Peptonic Medical AB
1 devices