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

BodySculp

K Number: K212331 · Decision Nov 9, 2021
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
18
Applicant Total
6
Review Days
105

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Basic Information

Device Name
BodySculp
K Number
K212331
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Rohrer Aesthetics, LLC
Date Received
July 27, 2021
Decision Date
November 9, 2021
Product Code
PKT
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
PKT Laser For Disruption Of Adipocyte Cells For Aesthetic Use

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