K-number	K123096
Device name	REPROCESSED VESSEL SEALER
Applicant	Sterilmed, Inc.
Product code	NUJ
Device class	Class II
Decision date	Jan 25, 2013
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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REPROCESSED VESSEL SEALER

Everything you need for a 510(k) submission. Nothing you don't.