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

REACTION SYSTEM

K Number: K090221 · Decision Jul 1, 2009
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
18
Applicant Total
11
Review Days
152

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Basic Information

Device Name
REACTION SYSTEM
K Number
K090221
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
Viora , Ltd.
Date Received
January 30, 2009
Decision Date
July 1, 2009
Product Code
NUV
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
NUV Massager, Vacuum, Light Induced Heating

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NUV), 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
K141904 VIORA V-TOUCH
K133837 VIORA V-TOTAL
K090399 TRIOS SYSTEM
Search all 11 clearances from Viora , Ltd. →