K240482

Intense Pulsed Light System (ST-690)

510(k) number
K240482
Device name
Intense Pulsed Light System (ST-690)
Applicant
Smedtrum Medical Technology Co., Ltd. TW
Product code
ONF — Powered Light Based Non-Laser Surgical Instrument Wi
Decision date
2024-05-17
Date received
2024-02-20
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain

Also available from FDA: K240482.pdf

Official FDA record: K240482
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.