K-number	K991591
Device name	BIOTHANE PATIENT RESTRAINT
Applicant	Bioplastics
Product code	FMQ
Device class	Class I
Decision date	Jul 29, 1999
Decision	Substantially Equivalent
Regulation	880.6760

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Source

View the full FDA submission: accessdata.fda.gov

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BIOTHANE PATIENT RESTRAINT

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