FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

SLIMUS

K Number: K192970 · Decision Dec 1, 2020
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
18
Applicant Total
8
Review Days
405

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
SLIMUS
K Number
K192970
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
Hironic Co., Ltd.
Date Received
October 23, 2019
Decision Date
December 1, 2020
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 Hironic Co., Ltd.

K Number Device Name
K260397 SYNERJET PRO (SP-1002); InPhiuse (SP-1002); WOWJET (SP-1002)
K251334 NEW DOUBLO 2.0
K241099 Plasonic (Plasonic)
K233123 SILKRO
K210084 SILKRO
K201773 PICOHI
K173676 A-FIT