K-number	K960508
Device name	PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25
Applicant	The Prometheus Group
Product code	HIR
Device class	Class II
Decision date	Jan 16, 1997
Decision	Substantially Equivalent
Regulation	884.1425

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View the full FDA submission: accessdata.fda.gov

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PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25

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