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Parker Quality & Compliance

PQC Reg Watch

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510(k) clearance

Diode Laser Therapy Systems (DL612A)

FDA 510(k) source

510(k) number
K262070
Applicant
Hebei Zollvan Medical Technology Co., Ltd.
Decision date
Aug 19, 2026
Date received
Jun 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
Baoding, CN