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

VENACURE EVLT NEVERTOUCH PROCEDURE KIT

K Number: K130671 · Decision Mar 26, 2013
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
58
Review Days
14

Basic Information

Device Name
VENACURE EVLT NEVERTOUCH PROCEDURE KIT
K Number
K130671
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ANGIODYNAMICS, INC.
Date Received
March 12, 2013
Decision Date
March 26, 2013
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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