K-number	K830705
Device name	MINI LANCET-BLOOD LANCET
Applicant	Pharmaquest Corp.
Product code	FMA
Device class	Class I
Decision date	Apr 8, 1983
Decision	Substantially Equivalent
Regulation	880.6230

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View the full FDA submission: accessdata.fda.gov

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MINI LANCET-BLOOD LANCET

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