K-number	K904295
Device name	PROGUARD(TM) BLOOD COLLECTION NEEDLE
Applicant	Safety-Ject, Inc.
Product code	FMI
Device class	Class II
Decision date	Oct 15, 1990
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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PROGUARD(TM) BLOOD COLLECTION NEEDLE

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