K-number	K812969
Device name	S/P CAPILLARY TUBES, HEPARINIZED (2A)
Applicant	American Dade
Product code	GIO
Device class	Class I
Decision date	Nov 6, 1981
Decision	Substantially Equivalent
Regulation	864.6150

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View the full FDA submission: accessdata.fda.gov

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S/P CAPILLARY TUBES, HEPARINIZED (2A)

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