Sensacare , Ltd. is one of 389 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Sensacare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SENSACARE MODEL SAA-102 ARM TYPE DIGITAL BLOOD PRESSURE MONITOR, SENSACARE SAW-102 WRIST DIGITAL BLOOD PRESSURE MONITOR
2
Total
2
Cleared
0
Denied
Sensacare , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Nei Hu, Taipei, TW.
Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sensacare , Ltd. 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 - Sensacare , Ltd.
2 devices