FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

ACRYDERM SILVER ANTI-MICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045

K Number: K991818 · Decision Apr 17, 2000
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
14
Review Days
326

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Basic Information

Device Name
ACRYDERM SILVER ANTI-MICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044, 1045
K Number
K991818
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acrymed, Inc.
Date Received
May 27, 1999
Decision Date
April 17, 2000
Product Code
FRO
Advisory Committee
Unknown
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
FRO Dressing, Wound, Drug

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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
K992032 ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033
Search all 14 clearances from Acrymed, Inc. →