K-number	K933791
Device name	PHILIPS ANGIOPRO RELEASE 2.1
Applicant	Philips Medical Systems North America, Inc.
Product code	JAA
Device class	Class II
Decision date	Nov 22, 1993
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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PHILIPS ANGIOPRO RELEASE 2.1

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