AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999— 510(k) K071120

Name: FDA 510(k) clearance K071120
Creator: U.S. Food and Drug Administration
Published: 2008-03-13

Substantially Equivalent

Aemed, Inc.

FDA 510(k) clearance K071120 for AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999, Substantially Equivalent on 2008-03-13. Applicant: Aemed, Inc.. Device class: 2.

Clearance details

Applicant: Aemed, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2007-04-20
Decision date: 2008-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South Miami, FL, US

Download summary PDF View on FDA.gov ↗

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