EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-201311— 510(k) K071320

Name: FDA 510(k) clearance K071320
Creator: U.S. Food and Drug Administration
Published: 2007-08-17

Substantially Equivalent

Everlife Medical Equipment Co., Ltd.

FDA 510(k) clearance K071320 for EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-201311, Substantially Equivalent on 2007-08-17. Applicant: Everlife Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Everlife Medical Equipment Co., Ltd.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 2007-05-10
Decision date: 2007-08-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu City, TW

Download summary PDF View on FDA.gov ↗

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