FDA 510(k), K111875, RELIEVA SPIN SINUS DILATION SYSTEM

FDA 510(k), K111875, RELIEVA SPIN SINUS DILATION SYSTEM

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510(K) Number: K111875
Device Name: RELIEVA SPIN SINUS DILATION SYSTEM
Manufacturer: ACCLARENT, INC.
Device Classification Name: instrument, ent manual surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 07/01/2011
Decision Date: 10/11/2011
Regulation Medical Specialty: Ear Nose & Throat

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