ACUTRON MULTIWAVE FOR USE IN TMJ SYNDROME PAIN CON— 510(k) K890143

Name: FDA 510(k) clearance K890143
Creator: U.S. Food and Drug Administration
Published: 1989-05-01

Substantially Equivalent

Microcurrent Research, Inc.

FDA 510(k) clearance K890143 for ACUTRON MULTIWAVE FOR USE IN TMJ SYNDROME PAIN CON, Substantially Equivalent on 1989-05-01. Applicant: Microcurrent Research, Inc.. Device class: 2.

Clearance details

Applicant: Microcurrent Research, Inc.
Product code: Code NUW
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1989-01-13
Decision date: 1989-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Haven, CT, US

Download summary PDF View on FDA.gov ↗

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