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

FERRIS DYNADERM PLUS

K Number: K865089 · Decision Feb 4, 1987
Classifications
1
FEI Numbers
384
Registration Numbers
385
Same Product Code
702
Applicant Total
20
Review Days
36

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Basic Information

Device Name
FERRIS DYNADERM PLUS
K Number
K865089
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent for Some Indications
Applicant
Ferris Mfg. Corp.
Date Received
December 30, 1986
Decision Date
February 4, 1987
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 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
Search all 20 clearances from Ferris Mfg. Corp. →