Tms Telemedizinische Systeme GmbH is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Tms Telemedizinische Systeme GmbH - FDA 510(k) Cleared Devices
Recent clearances: LOOP RECORDER VITAPHONE, 3100 SERIES, SENSOR MOBILE SM 100 VITAPHONE 1001R REMOS
2
Total
2
Cleared
0
Denied
Tms Telemedizinische Systeme GmbH has 2 FDA 510(k) cleared medical devices. Based in Chemnitz, DE.
Historical record: 2 cleared submissions from 2005 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tms Telemedizinische Systeme GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tms Telemedizinische Systeme GmbH
2 devices