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

Venus Legacy CX

K Number: K143554 · Decision Aug 4, 2015
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
9
Review Days
232

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Basic Information

Device Name
Venus Legacy CX
K Number
K143554
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
Venus Concept , Ltd.
Date Received
December 15, 2014
Decision Date
August 4, 2015
Product Code
PBX
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
PBX Massager, Vacuum, Radio Frequency Induced Heat

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K111670 VENUS FREEZE (MP)2 SYSTEM
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K100586 VENUS FREEZE SYSTEM