K-number	K953102
Device name	BLOODBORNE PATHOGEN KIT
Applicant	Certified Safety Mfg., Inc.
Product code	FXX
Device class	Class II
Decision date	Dec 11, 1995
Decision	Substantially Equivalent
Regulation	878.4040

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Source

View the full FDA submission: accessdata.fda.gov

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BLOODBORNE PATHOGEN KIT

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