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

ASPEN ESMARK BANDAGE

K Number: K872868 · Decision Jul 31, 1987
Classifications
1
FEI Numbers
681
Registration Numbers
681
Same Product Code
41
Applicant Total
55
Review Days
10

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Basic Information

Device Name
ASPEN ESMARK BANDAGE
K Number
K872868
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5075
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Aspen Laboratories, Inc.
Date Received
July 21, 1987
Decision Date
July 31, 1987
Product Code
FQM
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FQM Bandage, Elastic

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