K-number	K083060
Device name	REPROCESSED HARMONIC SCALPEL
Applicant	Sterilmed, Inc.
Product code	NLQ
Device class	Class U
Decision date	Jan 9, 2009
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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REPROCESSED HARMONIC SCALPEL

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