K-number	K904013
Device name	SPIVE NEEDLE SYSTEM, MODIFICATION
Applicant	Pascall Medical Corp.
Product code	FPA
Device class	Class II
Decision date	Oct 1, 1990
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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SPIVE NEEDLE SYSTEM, MODIFICATION

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