K-number	K800554
Device name	MULTI-FORMAT SFD MODEL 1720
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	IXL
Device class	Class II
Decision date	Apr 10, 1980
Decision	Substantially Equivalent
Regulation	892.1670

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View the full FDA submission: accessdata.fda.gov

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MULTI-FORMAT SFD MODEL 1720

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