Mks Paris is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Mks Paris - FDA 510(k) Cleared Devices
Recent clearances: ICE COMPRESSION FIRST, DUO, & MOOVE Systems
1
Total
1
Cleared
0
Denied
Mks Paris has 1 FDA 510(k) cleared medical devices. Based in Fabregues, FR.
Last cleared in 2021. Active since 2021. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Mks Paris Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by NJK & Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Mks Paris
1 devices