K-number	K896086
Device name	PROGUARD II(TM)
Applicant	Safety-Ject, Inc.
Product code	FMF
Device class	Class II
Decision date	Jan 24, 1990
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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PROGUARD II(TM)

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