EMJOI TENS DEVICE— 510(k) K052711

Substantially Equivalent

Emjoi, Inc.

FDA 510(k) clearance K052711 for EMJOI TENS DEVICE, Substantially Equivalent on 2006-06-23. Applicant: Emjoi, Inc.. Device class: 2.

Clearance details

Applicant: Emjoi, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2005-09-29
Decision date: 2006-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Midlothian, VA, US

Download summary PDF View on FDA.gov ↗

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