Hdc Corp. - FDA 510(k) Cleared Devices
30
Total
29
Cleared
0
Denied
Hdc Corp. has 29 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 29 cleared submissions from 1983 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hdc Corp. Filter by specialty or product code using the sidebar.
30 devices
Cleared
Nov 05, 2007
V-CATH POLY PICC
General Hospital
122d
Cleared
Mar 02, 2004
NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III...
Anesthesiology
512d
Cleared
Jan 14, 2004
MODIFICATION TO V-CATH POLY PICC
General Hospital
34d
Cleared
Sep 10, 2003
SELDINGER SAFETY NEEDLE INTRODUCER
Cardiovascular
37d
Cleared
Sep 09, 2003
PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09,...
Anesthesiology
386d
Cleared
Sep 20, 2002
SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S,...
General Hospital
85d
Cleared
Mar 15, 2001
EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)
Obstetrics & Gynecology
30d
Cleared
Oct 13, 2000
CLA KIT (CONTINUOUS LOCAL ANESTHESIA), MODEL 551-17, 551-10, 551-07
Anesthesiology
319d
Cleared
Sep 26, 2000
IBIS CHEMO-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, MODEL...
General Hospital
20d
Cleared
Mar 15, 1999
ENTERO-TEST HP, MODEL #102-01
Microbiology
188d
Cleared
Nov 23, 1998
V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER)
General Hospital
20d
Cleared
Oct 16, 1998
V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER) SEE APPENDIX 1
General Hospital
18d