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

ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033

K Number: K992032 · Decision Aug 19, 1999
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
14
Review Days
64

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Basic Information

Device Name
ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033
K Number
K992032
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acrymed, Inc.
Date Received
June 16, 1999
Decision Date
August 19, 1999
Product Code
KMF
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
KMF Bandage, Liquid

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Other Clearances by Acrymed, Inc.

K Number Device Name
K091354 ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSING
K083103 ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #B
K082459 ACRYDERM ABSORBENT OXYGEN DRESSING
K070333 ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GEL
K061232 ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006
K011994 ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101
K012116 ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSING
K002909 ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103
K002599 MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
K991818 ACRYDERM SILVER ANTI-MICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
Search all 14 clearances from Acrymed, Inc. →