Electrical Neuromuscular Stimulator, Cure Trio— 510(k) K233046

Name: FDA 510(k) clearance K233046
Creator: U.S. Food and Drug Administration
Published: 2024-04-19

Substantially Equivalent

Oriental Inspiration Limited

FDA 510(k) clearance K233046 for Electrical Neuromuscular Stimulator, Cure Trio, Substantially Equivalent on 2024-04-19. Applicant: Oriental Inspiration Limited. Device class: 2.

Clearance details

Applicant: Oriental Inspiration Limited
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2023-09-25
Decision date: 2024-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hong Kong, CN

Download summary PDF View on FDA.gov ↗

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