K-number	K180621
Device name	EchoMark, EchoMark LP
Applicant	Sonavex, Inc.
Product code	NEU
Device class	Class II
Decision date	Jun 6, 2018
Decision	Substantially Equivalent
Regulation	878.4300

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Source

View the full FDA submission: accessdata.fda.gov

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EchoMark, EchoMark LP

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