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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Diode Laser Hair Removal Machine (QDTM-03)

FDA 510(k) source

510(k) number
K261692
Applicant
Beijing Nubway S&T Co., Ltd.
Decision date
Oct 7, 2026
Date received
May 22, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
GEX
Device type
Powered Laser Surgical Instrument
Device class
Class II
Regulation
21 CFR 878.4810
Advisory committee
General, Plastic Surgery
Statement or summary
Summary
Third party
N
Location
Beijing, CN