K-number	K031876
Device name	ELECTRO FLO PERCUSSOR, MODEL 5000
Applicant	Med Systems
Product code	BYI
Device class	Class II
Decision date	Nov 21, 2003
Decision	Substantially Equivalent
Regulation	868.5665

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View the full FDA submission: accessdata.fda.gov

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ELECTRO FLO PERCUSSOR, MODEL 5000

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