Vitaphore Corp.
Vitaphore Corp. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1992.
Top product codes for Vitaphore Corp.
Recent clearances by Vitaphore Corp.
- K914579 — SILVER FOAM WOUND DRESSING
- K913148 — COLLAGEN SHIELD FOR ACUTE CARE
- K895920 — VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS
- K902558 — COLLAGEN SHIELD FOR ACUTE CARE
- K891993 — COLLAGEN NEUROSPONGE
- K896455 — VITACHOICE WOUND DRESSING
- K895993 — VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE
- K896046 — VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE
- K890435 — VITAACCESS CATHETER INTRODUCER KIT
- K882100 — VITACUFF(R) PERCUTANEOUS INFECT. CONTROL KIT
- K872998 — VITAACCESS (TM) CATHETER INTRODUCER SYSTEM
- K872538 — VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS
- K861563 — VITAGUARD PERCUTANEOUS INFECTION CONTROL KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.