K-number	K790953
Device name	BORDISPO BRAND HYPODERMIC NEEDLE
Applicant	Borda Products, Inc.
Product code	FMI
Device class	Class II
Decision date	Jun 27, 1979
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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BORDISPO BRAND HYPODERMIC NEEDLE

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