K-number	K810118
Device name	LS1000 ELECTRONIC FOCUS
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	IYN
Device class	Class II
Decision date	Feb 19, 1981
Decision	Substantially Equivalent
Regulation	892.1550

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View the full FDA submission: accessdata.fda.gov

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LS1000 ELECTRONIC FOCUS

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