ELECTROTHERAPY DEVICE (COMBO UNIT)— 510(k) K130691

Name: FDA 510(k) clearance K130691
Creator: U.S. Food and Drug Administration
Published: 2013-12-20

Substantially Equivalent

Guangzhou Finecure Medical Equipment Co.,Ltd

FDA 510(k) clearance K130691 for ELECTROTHERAPY DEVICE (COMBO UNIT), Substantially Equivalent on 2013-12-20. Applicant: Guangzhou Finecure Medical Equipment Co.,Ltd. Device class: 2.

Clearance details

Applicant: Guangzhou Finecure Medical Equipment Co.,Ltd
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2013-03-13
Decision date: 2013-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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