DIGITAL EMG MONITOR MYOTRON 120— 510(k) K882266

Substantially Equivalent

Ats Co.

FDA 510(k) clearance K882266 for DIGITAL EMG MONITOR MYOTRON 120, Substantially Equivalent on 1988-08-15. Applicant: Ats Co.. Device class: 2.

Clearance details

Applicant: Ats Co.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1988-05-31
Decision date: 1988-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Riverside, CA, 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.