K-number	K012579
Device name	REPROCESSED PHACO TIPS
Applicant	Sterilmed, Inc.
Product code	NKX
Device class	Class II
Decision date	Nov 8, 2001
Decision	Substantially Equivalent
Regulation	886.4670

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Source

View the full FDA submission: accessdata.fda.gov

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REPROCESSED PHACO TIPS

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