K-number	K043358
Device name	REPROCESSED ULTRASONIC SCALPELS
Applicant	Alliance Medical Corp.
Product code	NLQ
Device class	Class U
Decision date	Jun 6, 2005
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED ULTRASONIC SCALPELS

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