K-number	K890746
Device name	MYOTEST DBS NERVE STIMULATOR
Applicant	Biometer Intl. A/S
Product code	BXN
Device class	Class II
Decision date	Jul 14, 1989
Decision	Substantially Equivalent
Regulation	868.2775

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View the full FDA submission: accessdata.fda.gov

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MYOTEST DBS NERVE STIMULATOR

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