K-number	K905390
Device name	KUDO (POWERED ROTATION BED)
Applicant	Kinetic Concepts, Inc.
Product code	IKZ
Device class	Class II
Decision date	Jan 8, 1991
Decision	Substantially Equivalent
Regulation	890.5225

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View the full FDA submission: accessdata.fda.gov

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KUDO (POWERED ROTATION BED)

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