K-number	K192914
Device name	Stimuplex Onvision System
Applicant	Philips Medical Systems Nederland B.V.
Product code	BSP
Device class	Class II
Decision date	May 27, 2020
Decision	Substantially Equivalent
Regulation	868.5150

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Source

View the full FDA submission: accessdata.fda.gov

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Stimuplex Onvision System

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