K-number	K003987
Device name	URS-1K (KETONE TESST)
Applicant	Teco Diagnostics
Product code	JIN
Device class	Class I
Decision date	Apr 26, 2001
Decision	Substantially Equivalent
Regulation	862.1435

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View the full FDA submission: accessdata.fda.gov

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URS-1K (KETONE TESST)

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