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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)

FDA 510(k) source

510(k) number
K261582
Applicant
Zhengzhou PZ Laser Slim Technology Co., Ltd.
Decision date
Aug 28, 2026
Date received
May 13, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
NUV
Device type
Massager, Vacuum, Light Induced Heating
Device class
Class II
Regulation
21 CFR 878.4810
Advisory committee
General, Plastic Surgery
Statement or summary
Summary
Third party
N
Location
Zhengzhou, CN