K-number	K090940
Device name	SPOTCHECK BLOOD SPOT CONTROL, ASSAYED
Applicant	Astoria-Pacific, Inc.
Product code	JJT
Device class	Class I
Decision date	Dec 14, 2009
Decision	Substantially Equivalent
Regulation	862.1660

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View the full FDA submission: accessdata.fda.gov

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SPOTCHECK BLOOD SPOT CONTROL, ASSAYED

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