Carematix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BLIP MODEL BP-700WF
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Carematix, Inc. Cardiovascular ✕
5 devices
Cleared
Nov 28, 2012
BLIP MODEL BP-700WF
Cardiovascular
61d
Cleared
May 05, 2010
CAREMATIX WELLNESS SYSTEM, MODEL CWS-5000.1-B
Cardiovascular
72d
Cleared
Jan 11, 2008
CAREMATIX WELLNESS SYSTEM, MODEL CWS-5000.1-B
Cardiovascular
74d
Cleared
Jun 02, 2004
MODIFICATION TO CAREMATIX WELLNESS SYSTEM
Cardiovascular
49d
Cleared
Oct 10, 2003
CAREMATIX WELLNESS SYSTEM
Cardiovascular
116d