K-number	K030598
Device name	MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS
Applicant	Medisiss
Product code	NLQ
Device class	Class U
Decision date	Jan 23, 2004
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MEDISISS REPROCESSED ULTRASONIC SURGICAL INSTRUMENTS

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