K-number	K121929
Device name	ZEPHYR 'X-SERIES PATIENT TRANSFER SLED
Applicant	Diacor, Inc.
Product code	FRZ
Device class	Class II
Decision date	Jan 17, 2013
Decision	Substantially Equivalent
Regulation	880.6775

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Source

View the full FDA submission: accessdata.fda.gov

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ZEPHYR 'X-SERIES PATIENT TRANSFER SLED

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