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

VIORA V-TOUCH

K Number: K141904 · Decision Oct 21, 2014
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
11
Review Days
99

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Basic Information

Device Name
VIORA V-TOUCH
K Number
K141904
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
Viora , Ltd.
Date Received
July 14, 2014
Decision Date
October 21, 2014
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), ordered by most recent decision date.

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Other Clearances by Viora , Ltd.

K Number Device Name
K202247 V30 system, V20 system, V10 system, V-VR Hand piece
K201064 V30 System, V20 System, V10 System, V-FR Handpiece
K200468 V30 system, V20 system, V10 system, V-FC Handpiece
K162363 V30 system, V-Form Handpiece BC Medium applicator
K152611 V20 system
K150035 V10 system
K142093 V20 SYSTEM
K133837 VIORA V-TOTAL
K090221 REACTION SYSTEM
K090399 TRIOS SYSTEM
Search all 11 clearances from Viora , Ltd. →