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

PINXEL-RF system

K Number: K180654 · Decision Jul 13, 2018
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
6
Review Days
122

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Basic Information

Device Name
PINXEL-RF system
K Number
K180654
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
Rohrer Aesthetics, LLC
Date Received
March 13, 2018
Decision Date
July 13, 2018
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

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