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

FLEXIVA SF SIDE-FIRING SINGLE-USE LASER FIBER

K Number: K140503 · Decision Apr 15, 2014
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
29
Review Days
47

Basic Information

Device Name
FLEXIVA SF SIDE-FIRING SINGLE-USE LASER FIBER
K Number
K140503
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BOSTON SCIENTIFIC
Date Received
February 27, 2014
Decision Date
April 15, 2014
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

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