Intense Pulsed Light Treatment System (LK-PT)— 510(k) K242440

Name: FDA 510(k) clearance K242440
Creator: U.S. Food and Drug Administration
Published: 2024-11-14

Substantially Equivalent

Nanjing Bestview Laser S&T Co., Ltd.

FDA 510(k) clearance K242440 for Intense Pulsed Light Treatment System (LK-PT), Substantially Equivalent on 2024-11-14. Applicant: Nanjing Bestview Laser S&T Co., Ltd.. Device class: 2.

Clearance details

Applicant: Nanjing Bestview Laser S&T Co., Ltd.
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2024-08-16
Decision date: 2024-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nanjing, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.