Healthdyne Cardiovascular, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Healthdyne Cardiovascular, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Healthdyne Cardiovascular, Inc. has 4 FDA 510(k) cleared medical devices. Based in Costa Mesa, US.
Historical record: 4 cleared submissions from 1989 to 1990. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Healthdyne Cardiovascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Healthdyne Cardiovascular, Inc.
5 devices
Cleared
Jul 25, 1990
ISOFLO(TM) AMNIOCENTESIS TRAY
Obstetrics & Gynecology
107d
Cleared
Jul 19, 1990
ISOFLO(TM) HIGH PRESSURE INJECTION LINES
Cardiovascular
119d
Cleared
Jun 01, 1990
ISOFLO INTRAUTERINE PRESSURE MONITORING & AMNIO.
Obstetrics & Gynecology
86d
Cleared
May 14, 1990
DRESSING CHANGE KIT
General Hospital
90d
Cleared
Dec 22, 1989
ISOFLO AND ISOTEC INTRAUTERINE PRESSURE MONITORING
Obstetrics & Gynecology
87d