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

DERMISTRIP

K Number: K861972 · Decision Jun 27, 1986
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
12
Review Days
37

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Basic Information

Device Name
DERMISTRIP
K Number
K861972
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4020
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent for Some Indications
Applicant
Kells Medical, Inc.
Date Received
May 21, 1986
Decision Date
June 27, 1986
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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K926333 CPR PLUS
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K890094 EVA EMPTY SOLUTION CONTAINER W/3 LEAD TRANSFER SET
K844463 DERMIDRESS
K844072 DERMIZIP SKIN CLOSURE DEVICE
K832678 PHONATORY FUNCTION ANALYZER PS-77
K832667 LUCAE'S EAR & NASAL APPLICATORS
K823118 SAY
K823226 SN-100 DOCTOR'S ROUND
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