Medical Device Manufacturer · US , Walker , MI

Hdc Corp. - FDA 510(k) Cleared Devices

30 submissions · 29 cleared · Since 1983

30

Total

29

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hdc Corp. General Hospital ✕

16 devices

1-16 of 16

Cleared Nov 05, 2007

V-CATH POLY PICC

General Hospital · 122d

Cleared Jan 14, 2004

MODIFICATION TO V-CATH POLY PICC

General Hospital · 34d

Cleared Sep 20, 2002

SAFE-T-PEEL SAFETY NEEDLE/INTRODUCER, MODELS 350-300 S,...

General Hospital · 85d

Cleared Sep 26, 2000

IBIS CHEMO-PORT IMPLANTABLE VASCULAR ACCESS SYSTEM, MODEL...

General Hospital · 20d

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

Cleared Mar 05, 1997

General Hospital · 84d

Cleared Apr 30, 1996

V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER

General Hospital · 291d

Cleared Jun 23, 1995

V-CATH PERCUTANEOUS INTRODUCER KIT

General Hospital · 88d

Cleared Jun 02, 1995

HDC VADD (VASCULAR ACCESS DEVICE) TUNNELER

General Hospital · 85d

Cleared Jan 20, 1995

V-CATH BREAKAWAY NEEDLE INTRODUCER

General Hospital · 73d

Cleared Jan 10, 1992

General Hospital · 165d

Cleared Dec 30, 1987

General Hospital · 77d

Cleared Dec 03, 1987

CHEMO-PORT NON-CORING NEEDLES

General Hospital · 114d

Cleared Jul 17, 1986

HDC CHEMO-PORT (VASCULAR)

General Hospital · 343d

Cleared Mar 06, 1984

General Hospital · 99d