K-number	K811225
Device name	HUMAN BLOOD IN ALSEVER'S
Applicant	Dutchland Laboratories, Inc.
Product code	JSK
Device class	Class I
Decision date	Jun 12, 1981
Decision	Substantially Equivalent
Regulation	866.2450

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View the full FDA submission: accessdata.fda.gov

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HUMAN BLOOD IN ALSEVER'S

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