K-number	K190624
Device name	EarlyVue VS30
Applicant	Philips Medizin Systeme Boeblingen GmbH
Product code	DSJ
Device class	Class II
Decision date	Oct 27, 2019
Decision	Substantially Equivalent
Regulation	870.1100

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Source

View the full FDA submission: accessdata.fda.gov

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EarlyVue VS30

Everything you need for a 510(k) submission. Nothing you don't.