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

COLLAGEN SHIELD FOR ACUTE CARE

K Number: K902558 · Decision Aug 17, 1990
Classifications
1
FEI Numbers
11
Registration Numbers
12
Same Product Code
18
Applicant Total
13
Review Days
67

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Basic Information

Device Name
COLLAGEN SHIELD FOR ACUTE CARE
K Number
K902558
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
886.4750
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
Vitaphore Corp.
Date Received
June 11, 1990
Decision Date
August 17, 1990
Product Code
MOE
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
MOE Collagen Corneal Shield

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Other Clearances by Vitaphore Corp.

K Number Device Name
K914579 SILVER FOAM WOUND DRESSING
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K891993 COLLAGEN NEUROSPONGE
K896455 VITACHOICE WOUND DRESSING
K896046 VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE
K895993 VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE
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. →