Rossmax Internationl , Ltd. is one of 363 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Rossmax Internationl , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ROSSMAX DIGITAL SPHYGMOMANOMETER MANDAUS II
4
Total
4
Cleared
0
Denied
Rossmax Internationl , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Historical record: 4 cleared submissions from 2001 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rossmax Internationl , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Center For Measurement Standards of Industrial as regulatory consultant.
FDA 510(k) Regulatory Record - Rossmax Internationl , Ltd.
4 devices
Cleared
Feb 03, 2006
ROSSMAX DIGITAL SPHYGMOMANOMETER MANDAUS II
Cardiovascular
100d
Cleared
Aug 06, 2002
ROSSMAX AUTOMATIC WRIST BLOOD PRESSURE MONITOR, MODELS B150 & Q400
Cardiovascular
140d
Cleared
Mar 20, 2001
WRISTWATCH BLOOD PRESSURE MONITOR A46
Cardiovascular
27d
Cleared
Feb 08, 2001
WRISTWATCH BLOOD PRESSURE MONITOR, MODEL A43
Cardiovascular
17d