K-number	K890555
Device name	PATIENT MOVER(TM)
Applicant	T.B.S., Inc.
Product code	ILK
Device class	Class II
Decision date	Feb 13, 1989
Decision	Substantially Equivalent
Regulation	890.5150

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View the full FDA submission: accessdata.fda.gov

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PATIENT MOVER(TM)

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