K-number	K960809
Device name	PHILIPS SITE VIEW WORKSTATION
Applicant	Philips Medical Systems North America, Inc.
Product code	LMD
Device class	Class I
Decision date	Apr 7, 1996
Decision	Substantially Equivalent
Regulation	892.2020

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View the full FDA submission: accessdata.fda.gov

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PHILIPS SITE VIEW WORKSTATION

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