Medical Device Manufacturer · US , San Francisco , CA

Vitaphore Corp. - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 1986

13

Total

12

Cleared

0

Denied

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

6 devices

1-6 of 6

Cleared Jan 11, 1990

VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE

General Hospital · 90d

Cleared Jan 11, 1990

VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE

General Hospital · 86d

Cleared Mar 29, 1989

VITAACCESS CATHETER INTRODUCER KIT

General Hospital · 61d

Cleared Jul 13, 1988

VITACUFF(R) PERCUTANEOUS INFECT. CONTROL KIT

General Hospital · 55d

Cleared Mar 24, 1988

VITAACCESS (TM) CATHETER INTRODUCER SYSTEM

General Hospital · 234d

Cleared Aug 27, 1986

VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT

General Hospital · 124d