K-number	K820625
Device name	HEMALET AUTOMATIC LANCET DEVICE
Applicant	Medprobe Laboratories
Product code	FMK
Device class	Class II
Decision date	Apr 9, 1982
Decision	Substantially Equivalent
Regulation	878.4850

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View the full FDA submission: accessdata.fda.gov

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HEMALET AUTOMATIC LANCET DEVICE

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