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

MRDH BANDAGE

K Number: K082703 · Decision Oct 14, 2008
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
8
Review Days
28

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Basic Information

Device Name
MRDH BANDAGE
K Number
K082703
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Marine Polymer Technologies, Inc.
Date Received
September 16, 2008
Decision Date
October 14, 2008
Product Code
KMF
Advisory Committee
General Hospital
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
KMF Bandage, Liquid

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