HI-EMT MAGSHAPE— 510(k) K230024

Name: FDA 510(k) clearance K230024
Creator: U.S. Food and Drug Administration
Published: 2023-09-06

Substantially Equivalent

Beijing Sano Laser S&T Development Co.,Ltd

FDA 510(k) clearance K230024 for HI-EMT MAGSHAPE, Substantially Equivalent on 2023-09-06. Applicant: Beijing Sano Laser S&T Development Co.,Ltd. Device class: 2.

Clearance details

Applicant: Beijing Sano Laser S&T Development Co.,Ltd
Product code: Product code NGX
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2023-01-04
Decision date: 2023-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bejing, 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.