K-number	K905053
Device name	STAGE ZERO AIR FLOTATION BED
Applicant	Lake Medical Products, Inc.
Product code	IOQ
Device class	Class II
Decision date	Nov 26, 1990
Decision	Substantially Equivalent
Regulation	890.5170

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View the full FDA submission: accessdata.fda.gov

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STAGE ZERO AIR FLOTATION BED

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