K-number	K771824
Device name	MEDPRO FLOTATION SYSTEM
Applicant	Medpro, Inc.
Product code	IKY
Device class	Class I
Decision date	Oct 19, 1977
Decision	Substantially Equivalent
Regulation	880.5150

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View the full FDA submission: accessdata.fda.gov

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MEDPRO FLOTATION SYSTEM

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