K-number	K810183
Device name	PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	IZI
Device class	Class II
Decision date	Feb 25, 1981
Decision	Substantially Equivalent
Regulation	892.1600

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View the full FDA submission: accessdata.fda.gov

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PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION

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