Huntleigh Healthcare, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Huntleigh Healthcare, Inc. has 14 FDA 510(k) cleared medical devices. Based in Eatontown, US.
Historical record: 14 cleared submissions from 1993 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Huntleigh Healthcare, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Nov 18, 2004
IOP8 INTRA OPERATIVE PROBE
Radiology
479d
Cleared
Sep 19, 2002
DVT60
Cardiovascular
28d
Cleared
Mar 26, 2002
FLOWTRON UNIVERSAL, MODEL AC600
Cardiovascular
378d
Cleared
Sep 21, 2001
STS RANGE , MODELS STS20,STS30,STS40
Cardiovascular
86d
Cleared
May 02, 2001
VASCULAR ASSIST
Cardiovascular
286d
Cleared
Apr 25, 2001
BABY DOPPLEX 3000 MK 2 (BD3000)
Obstetrics & Gynecology
30d
Cleared
Apr 25, 2001
BABY DOPPLEX 3002 (BD3002)
Obstetrics & Gynecology
30d
Cleared
Sep 19, 2000
BABY DOPPLEX 4002-TWINS, MODEL BD4002
Obstetrics & Gynecology
90d
Cleared
Jan 24, 2000
BABY DOPPLEX 4000, MODEL BD 4000
Obstetrics & Gynecology
335d
Cleared
Jan 12, 1999
MODIFICATION OF: RHEO DOPPLEX II
Radiology
41d
Cleared
Jan 26, 1998
HUNTLEIGH FP5000 SYSTEM MODEL FP5000
Cardiovascular
399d
Cleared
Sep 12, 1997
BABY DOPPLEX (3000)
Obstetrics & Gynecology
361d
Cleared
Jun 24, 1994
MULTI DOPPLEX II / FETAL DOPPLEX II
Radiology
526d
Cleared
May 07, 1993
CALF GARMENT DVT10(S) COMPRESSIBLE LIMB SLEEVE
Cardiovascular
176d