K-number	K062604
Device name	RAPIDTEG TEG-ACT TEST
Applicant	Haemoscope Corp.
Product code	JBP
Device class	Class II
Decision date	Jan 31, 2007
Decision	Substantially Equivalent
Regulation	864.7140

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View the full FDA submission: accessdata.fda.gov

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RAPIDTEG TEG-ACT TEST

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