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

BAND-AID BRAND TRICOT MESH BANDAGES

K Number: K801823 · Decision Aug 20, 1980
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
5
Applicant Total
206
Review Days
20

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Basic Information

Device Name
BAND-AID BRAND TRICOT MESH BANDAGES
K Number
K801823
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4100
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Johnson & Johnson Professionals, Inc.
Date Received
July 31, 1980
Decision Date
August 20, 1980
Product Code
KGY
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
KGY Bag, Intestine

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