K-number	K895635
Device name	MYOSYSTEM 1000 ELECTROMYOGRAPH
Applicant	Noraxon USA, Inc.
Product code	HCC
Device class	Class II
Decision date	Apr 19, 1990
Decision	Substantially Equivalent
Regulation	882.5050

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View the full FDA submission: accessdata.fda.gov

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MYOSYSTEM 1000 ELECTROMYOGRAPH

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