K-number	K142022
Device name	MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES
Applicant	Medline Renewal
Product code	NLY
Device class	Class I
Decision date	Dec 19, 2014
Decision	Substantially Equivalent
Regulation	874.4140

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View the full FDA submission: accessdata.fda.gov

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MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES

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