K-number	K223770
Device name	Sonopet 1Q 3 7cm 1Q Large
Applicant	Stryker Corporation
Product code	LFL
Device class	Class U
Decision date	Feb 16, 2023
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Sonopet 1Q 3 7cm 1Q Large

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