Hdc Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
33
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K091390HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2July 30, 2009
K071875V-CATH POLY PICCNovember 5, 2007
K071851HDC STERILE SPIDER SCREWOctober 18, 2007
K052471HDC SPIDER SCREWDecember 23, 2005
K023342NEURO-TRACE III KIT, NEURO-TRACE III REGIONAL BLOCK CABLE, NEURO-TRACE III NERVE MAPPING PROBE, NEURMarch 2, 2004
K033853MODIFICATION TO V-CATH POLY PICCJanuary 14, 2004
K032404SELDINGER SAFETY NEEDLE INTRODUCERSeptember 10, 2003
K022752PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562September 9, 2003
K022099SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S, 360-300'S,380-300'S,390-300'SSeptember 20, 2002
K010425EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)March 15, 2001
K994059CLA KIT (CONTINUOUS LOCAL ANESTHESIA), MODEL 551-17, 551-10, 551-07October 13, 2000
K002770IBIS CHEMO-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, MODEL 700-08-10,700-08-11,700-08-12,700-08-15,70September 26, 2000
K983119ENTERO-TEST HP, MODEL #102-01March 15, 1999
K983916V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER)November 23, 1998
K983409V-CATH PICC (PERIPHERALLY INSERTED CENTRAL CATHETER) SEE APPENDIX 1October 16, 1998
K964966V-CATHMarch 5, 1997
K953300V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETERApril 30, 1996
K951384V-CATH PERCUTANEOUS INTRODUCER KITJune 23, 1995
K951098HDC VADD (VASCULAR ACCESS DEVICE) TUNNELERJune 2, 1995
K945473V-CATH BREAKAWAY NEEDLE INTRODUCERJanuary 20, 1995