K-number	K230472
Device name	Sonopuls 190
Applicant	Enraf-Nonius, B.V.
Product code	IMI
Device class	Class II
Decision date	Oct 24, 2023
Decision	Substantially Equivalent
Regulation	890.5300

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Source

View the full FDA submission: accessdata.fda.gov

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Sonopuls 190

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