FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VITACHOICE WOUND DRESSING

K Number: K896455 · Decision Feb 15, 1990
Classifications
1
FEI Numbers
934
Registration Numbers
934
Same Product Code
183
Applicant Total
13
Review Days
98

Basic Information

Device Name
VITACHOICE WOUND DRESSING
K Number
K896455
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
VITAPHORE CORP.
Date Received
November 9, 1989
Decision Date
February 15, 1990
Product Code
KGX
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGX Tape And Bandage, Adhesive

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Other Clearances by VITAPHORE CORP.

K Number Device Name
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
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
Search all 13 clearances from VITAPHORE CORP. →