MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES— 510(k) K142022

Name: FDA 510(k) clearance K142022
Creator: U.S. Food and Drug Administration
Published: 2014-12-19

Substantially Equivalent

Medline Renewal

FDA 510(k) clearance K142022 for MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES, Substantially Equivalent on 2014-12-19. Applicant: Medline Renewal. Device class: 1.

Clearance details

Applicant: Medline Renewal
Product code: Code NLY
Device class: Class 1
Regulation: 21 CFR 874.4140
Advisory panel: Ear, Nose, Throat
Date received: 2014-07-25
Decision date: 2014-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, OR, US

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