K-number	K870770
Device name	TIMLEINE(TM) VENIPUNCTURE SYSTEM
Applicant	Ipax, Inc.
Product code	KMK
Device class	Class I
Decision date	Apr 23, 1987
Decision	Substantially Equivalent
Regulation	880.5210

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View the full FDA submission: accessdata.fda.gov

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TIMLEINE(TM) VENIPUNCTURE SYSTEM

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