FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

TRANSCEND

K Number: K120510 · Decision Jul 19, 2013
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
35
Review Days
514

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Basic Information

Device Name
TRANSCEND
K Number
K120510
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Syneron Medical, Ltd.
Date Received
February 21, 2012
Decision Date
July 19, 2013
Product Code
GEI
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
GEI Electrosurgical, Cutting & Coagulation & Accessories

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