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

The Cellfina System

K Number: K192185 · Decision Oct 9, 2019
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
8
Applicant Total
14
Review Days
58

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Basic Information

Device Name
The Cellfina System
K Number
K192185
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4790
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ulthera, Inc.
Date Received
August 12, 2019
Decision Date
October 9, 2019
Product Code
OUP
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
OUP Powered Surgical Instrument For Improvement In The Appearance Of Cellulite

Similar 510(k) Clearances

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

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Other Clearances by Ulthera, Inc.

K Number Device Name
K260618 Ulthera® System
K250418 Ulthera System (UC-1 Control Unit PRIME Model 2.1)
K243035 Ulthera® System
K233996 Ulthera System (UC-1 Control Unit PRIME)
K180623 Ulthera System
K161885 The Cellfina System
K153677 The Cellfina System
K150505 Cellfina System
K134032 ULTHERA SYSTEM
K132028 ULTHERA SYSTEM
Search all 14 clearances from Ulthera, Inc. →