K-number	K901026
Device name	MJ PERCUSSOR(TM)
Applicant	Merced Medical, Inc.
Product code	BYI
Device class	Class II
Decision date	Mar 15, 1990
Decision	Substantially Equivalent
Regulation	868.5665

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View the full FDA submission: accessdata.fda.gov

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MJ PERCUSSOR(TM)

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