J4 MYO-MONITOR— 510(k) K842223

Substantially Equivalent

Myo-Tronics Research, Inc.

FDA 510(k) clearance K842223 for J4 MYO-MONITOR, Substantially Equivalent on 1984-11-19. Applicant: Myo-Tronics Research, Inc.. Device class: 2.

Clearance details

Applicant: Myo-Tronics Research, Inc.
Product code: Code NUW
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1984-06-05
Decision date: 1984-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.