FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Diosculpt

K Number: K222265 · Decision Sep 23, 2022
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
18
Applicant Total
6
Review Days
57

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Diosculpt
K Number
K222265
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
Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd
Date Received
July 28, 2022
Decision Date
September 23, 2022
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

Similar 510(k) Clearances

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

View all

Other Clearances by Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd

K Number Device Name
K243037 Diode Laser System model Dawn-S
K232885 Dawn Diode Laser System
K183122 810nm Diode Laser System
K163655 Sparkling
K161356 Matrix LS-40 CO2 Laser System