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

DYNAFILM

K Number: K874478 · Decision Jan 14, 1988
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
20
Review Days
73

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Basic Information

Device Name
DYNAFILM
K Number
K874478
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4020
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent for Some Indications
Applicant
Ferris Mfg. Corp.
Date Received
November 2, 1987
Decision Date
January 14, 1988
Product Code
NAD
Advisory Committee
General, Plastic Surgery
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
NAD Dressing, Wound, Occlusive

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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
K990906 FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
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
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