K-number	K001690
Device name	PROTECTIV SAFETY BLOOD COLLECTION NEEDLE
Applicant	Johnson & Johnson Medical, Inc.
Product code	FMI
Device class	Class II
Decision date	Jul 31, 2000
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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PROTECTIV SAFETY BLOOD COLLECTION NEEDLE

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