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

MODIFIED LYOFOAM WOUND DRESSINGS

K Number: K895764 · Decision Sep 10, 1990
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
27
Review Days
349

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Basic Information

Device Name
MODIFIED LYOFOAM WOUND DRESSINGS
K Number
K895764
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent for Some Indications
Applicant
Acme United Corp.
Date Received
September 26, 1989
Decision Date
September 10, 1990
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 Acme United Corp.

K Number Device Name
K961323 LYOFOAM EXTRA C ODOR ABSORBING WOUND DRESSING
K961452 LYOFOAM EXTRA 'A' STERILE ADHESIVE WOUND DRESSING
K952565 LYOFOAM EXTRA
K871740 LYOSHEET SURGICAL SHEET FOR BURNS
K864084 LYOFOAM C ODOR-ABSORBING DRESSING
K860085 LYOFOAM WOUND DRESSINGS
K860818 ONE TIME ENTERAL FEEDING BAG
K861015 ONE TIME HYPERAL & CATHETER DRESSING CHANGE TRAYS
K842186 ACU-DERM TRANSPARENT WOUND DRESSING
K842064 ACU-DERM TRANSPARENT IV DRESSING
Search all 27 clearances from Acme United Corp. →