K6-I DIAGNOSTIC SYSTEM— 510(k) K922456

Name: FDA 510(k) clearance K922456
Creator: U.S. Food and Drug Administration
Published: 1994-06-09

Substantially Equivalent for Some Indications

Myo-Tronics, Inc.

FDA 510(k) clearance K922456 for K6-I DIAGNOSTIC SYSTEM, Substantially Equivalent for Some Indications on 1994-06-09. Applicant: Myo-Tronics, Inc.. Device class: 2.

Clearance details

Applicant: Myo-Tronics, Inc.
Product code: Code KZM
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1992-05-26
Decision date: 1994-06-09
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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