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

VISIONARY 2000

K Number: K000639 · Decision May 25, 2000
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
73
Applicant Total
15
Review Days
90

Basic Information

Device Name
VISIONARY 2000
K Number
K000639
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BURTON MEDICAL PRODUCTS CORP.
Date Received
February 25, 2000
Decision Date
May 25, 2000
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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