K-number	K900460
Device name	MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER
Applicant	Novoste Corp.
Product code	DQO
Device class	Class II
Decision date	Jul 17, 1990
Decision	Substantially Equivalent
Regulation	870.1200

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View the full FDA submission: accessdata.fda.gov

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MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER

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