FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PROXENON 350, MODEL 902XX

K Number: K071218 · Decision Jun 14, 2007
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
44
Applicant Total
111
Review Days
43

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Basic Information

Device Name
PROXENON 350, MODEL 902XX
K Number
K071218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Welch Allyn, Inc.
Date Received
May 2, 2007
Decision Date
June 14, 2007
Product Code
FST
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
FST Light, Surgical, Fiberoptic

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