ESG-1 ELECTROSONOGRAM (ESG-1)— 510(k) K970116

Name: FDA 510(k) clearance K970116
Creator: U.S. Food and Drug Administration
Published: 1997-04-02

Substantially Equivalent

Myo-Tronics, Inc.

FDA 510(k) clearance K970116 for ESG-1 ELECTROSONOGRAM (ESG-1), Substantially Equivalent on 1997-04-02. Applicant: Myo-Tronics, Inc.. Device class: 1.

Clearance details

Applicant: Myo-Tronics, Inc.
Product code: Code NFQ
Device class: Class 1
Regulation: 21 CFR 872.2050
Advisory panel: Dental
Date received: 1997-01-13
Decision date: 1997-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tukwila, WA, US

Download summary PDF View on FDA.gov ↗

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K905449 — ELECTROSONOGRAM ESG-11991-04-26
K862286 — ARTHROPHONOMETER1987-01-07

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