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

AIM 200, MAJOR SURGICAL LIGHT

K Number: K101537 · Decision Sep 30, 2010
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
73
Applicant Total
15
Review Days
119

Basic Information

Device Name
AIM 200, MAJOR SURGICAL LIGHT
K Number
K101537
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
BURTON MEDICAL PRODUCTS CORP.
Date Received
June 3, 2010
Decision Date
September 30, 2010
Product Code
FSY
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
FSY Light, Surgical, Ceiling Mounted

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