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

RDH BANDAGE

K Number: K002550 · Decision Dec 20, 2000
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
8
Review Days
125

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Basic Information

Device Name
RDH BANDAGE
K Number
K002550
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5090
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Marine Polymer Technologies, Inc.
Date Received
August 17, 2000
Decision Date
December 20, 2000
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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K972914 SYVEK PATCH