Galix Biomedical Instrumentation, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Galix Biomedical Instrumentation, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Galix Biomedical Instrumentation, Inc. has 6 FDA 510(k) cleared medical devices. Based in Miami Beach, US.
Historical record: 6 cleared submissions from 1998 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Galix Biomedical Instrumentation, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Galix Biomedical Instrumentation, Inc.
6 devices
Cleared
Jul 09, 2010
3 CHANNEL DIGITAL AMBULATORY ECG RECORDER MODEL GALIX GBI-3SM
Cardiovascular
296d
Cleared
Jan 31, 2006
GALIX ECG PROFESSIONAL STATION
Cardiovascular
271d
Cleared
Sep 17, 2003
GALIX WINTER
Cardiovascular
245d
Cleared
Jun 11, 2003
GALIX PACESTAR
Cardiovascular
267d
Cleared
Mar 15, 2001
GALIX GBI -3S-LP
Cardiovascular
581d
Cleared
Jan 29, 1998
3 CHANNEL DIGITAL AMBULATORY ECG RECORDER
Cardiovascular
268d