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

Ultimate Contour, Ultimate Contour Mini

K Number: K171052 · Decision Oct 20, 2017
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
31
Review Days
193

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Basic Information

Device Name
Ultimate Contour, Ultimate Contour Mini
K Number
K171052
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
CAO Group, Inc.
Date Received
April 10, 2017
Decision Date
October 20, 2017
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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