K-number	K882266
Device name	DIGITAL EMG MONITOR MYOTRON 120
Applicant	Ats Co.
Product code	HCC
Device class	Class II
Decision date	Aug 15, 1988
Decision	Substantially Equivalent
Regulation	882.5050

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View the full FDA submission: accessdata.fda.gov

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DIGITAL EMG MONITOR MYOTRON 120

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