Vasomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VASOMEDICAL-BIOX 12- CHANNEL AMBULATORY ECG HOLTER RECORDER MODEL 1304, VASOMEDICAL-BIOX 3- CHANNEL MINIATURE AMBULATORY, VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE RECORDER MODEL 2302, VASOMEDICAL-BIOX AMBULATORY
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vasomedical, Inc. Cardiovascular ✕
7 devices
Cleared
Jun 28, 2011
VASOMEDICAL-BIOX 12- CHANNEL AMBULATORY ECG HOLTER RECORDER MODEL 1304,...
Cardiovascular
62d
Cleared
Jun 24, 2011
VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE...
Cardiovascular
65d
Cleared
Apr 02, 2010
COMBINED VASOMEDICAL-BIOX AMBULATORY ECG & BLOOD PRESSURE RECORDER & ANALYSIS...
Cardiovascular
204d
Cleared
Apr 01, 2009
VASOMEDICAL BIOX CB-1305-C, 3 CHANNEL ECG HOLTER MONITOR, MODEL CB-1305-C
Cardiovascular
100d
Cleared
Mar 01, 2004
EECP THERAPY SYSTEM MODEL TS4 WITH/WITHOUT PLUSE OXIMETRY
Cardiovascular
104d
Cleared
Jun 14, 2002
EECP THERAPY SYSTEM MODEL TS3 WITH PULSE OXIMETRY AND ENHANCED EXTERNAL...
Cardiovascular
88d
Cleared
Dec 06, 2000
EECP THERAPY SYSTEM, MODEL TS3
Cardiovascular
28d