K-number	K003824
Device name	OMNISONICS ULTRASONIC SURGERY SYSTEM, MODEL STI
Applicant	Omnisonics Medical Technologies
Product code	LFL
Device class	Class U
Decision date	Mar 8, 2001
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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OMNISONICS ULTRASONIC SURGERY SYSTEM, MODEL STI

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