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

AMSCO HARMONY SURGICAL LIGHTING AND MEDIA SYSTEM

K Number: K013242 · Decision Dec 13, 2001
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
28
Applicant Total
169
Review Days
76

Basic Information

Device Name
AMSCO HARMONY SURGICAL LIGHTING AND MEDIA SYSTEM
K Number
K013242
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STERIS Corporation
Date Received
September 28, 2001
Decision Date
December 13, 2001
Product Code
FTD
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
FTD Lamp, Surgical

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