K-number	K823583
Device name	MYOTEST NERVE STIMULATOR
Applicant	Prothia USA, Inc.
Product code	BXN
Device class	Class II
Decision date	Dec 30, 1982
Decision	Substantially Equivalent
Regulation	868.2775

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View the full FDA submission: accessdata.fda.gov

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MYOTEST NERVE STIMULATOR

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