Belimed Sauter AG is one of 140 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Belimed Sauter AG - FDA 510(k) Cleared Devices
Recent clearances: BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6, BELIMED STEAM STERILIZER TOP 5000, SERIES 8, MODELS: 6-0-12 VS1 AND VS2, BELIMED STEAM STERILIZER MODEL TOP 5000 SERIES 24
3
Total
3
Cleared
0
Denied
Belimed Sauter AG has 3 FDA 510(k) cleared medical devices. Based in Sulgen (Tg), CH.
Historical record: 3 cleared submissions from 2007 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Belimed Sauter AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Belimed Sauter AG
3 devices