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

FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER

K Number: K990906 · Decision Apr 29, 1999
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
20
Review Days
42

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Basic Information

Device Name
FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
K Number
K990906
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent for Some Indications
Applicant
Ferris Mfg. Corp.
Date Received
March 18, 1999
Decision Date
April 29, 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 Ferris Mfg. Corp.

K Number Device Name
K031660 FERRIS POLYMEM STERILE BREAST PAD
K031307 FERRIS POLYMEM SILVER WOUND DRESSING
K002129 FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGEN
K991729 FERRIS POLYOSTOMY STERILE WOUND DRESSING
K984539 FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING
K982306 POLYTUBE
K932913 FERRIS POLYMEM HYDROPHILIC WOUND DRESSING
K900127 FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)
K880330 FERRIS HYDROPHILIC DRESSING
K874478 DYNAFILM
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