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FDA 510(k), K061903, RELIEVA SINUS BALLOON CATHETER
FDA 510(k), K061903, RELIEVA SINUS BALLOON CATHETER
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510(K) Number: K061903
Device Name: RELIEVA SINUS BALLOON CATHETER
Manufacturer: ACCLARENT, INC.
Device Classification Name: instrument, ent manual surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 07/05/2006
Decision Date: 08/18/2006
Regulation Medical Specialty: Ear Nose & Throat
Device Name: RELIEVA SINUS BALLOON CATHETER
Manufacturer: ACCLARENT, INC.
Device Classification Name: instrument, ent manual surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 07/05/2006
Decision Date: 08/18/2006
Regulation Medical Specialty: Ear Nose & Throat
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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