FDA 510(k), K132440, XPRESS MULTI-SINUS DILATION TOOL

FDA 510(k), K132440, XPRESS MULTI-SINUS DILATION TOOL

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510(K) Number: K132440
Device Name: XPRESS MULTI-SINUS DILATION TOOL
Manufacturer: Entellus Medical, Inc.
Device Classification Name: instrument, ent manual surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 08/06/2013
Decision Date: 10/04/2013
Regulation Medical Specialty: Ear Nose & Throat

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