K-number	K961217
Device name	BODILY FLUID DISPOSAL KIT
Applicant	Transidyne General Corp.
Product code	FXX
Device class	Class II
Decision date	Jul 25, 1996
Decision	Substantially Equivalent
Regulation	878.4040

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View the full FDA submission: accessdata.fda.gov

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BODILY FLUID DISPOSAL KIT

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