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

ADHESIVE WOUND COVER FILM

K Number: K822080 · Decision Oct 15, 1982
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
85
Review Days
92

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Basic Information

Device Name
ADHESIVE WOUND COVER FILM
K Number
K822080
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4020
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Hollister, Inc.
Date Received
July 15, 1982
Decision Date
October 15, 1982
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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K083153 ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007
K050483 EVADRI BLADDER CONTROL SYSTEMS
K040779 RESTORE WOUND CLEANSER
K013612 INCARE PELVIC FLOOR THERAPY SYSTEM
K013653 INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE
K013483 INCARE ADVANCE; INTERMITTENT CATHETER, PLUS INTERMITTENT CATHETER, PLUS KIT
K013345 INCARE INTERMITTENT CATHETER
Search all 85 clearances from Hollister, Inc. →