• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K110739, ENTELLUS MEDICAL SINUS GUIDEWIRE, by Entellus Medical, Inc.

FDA 510(k) K110739, ENTELLUS MEDICAL SINUS GUIDEWIRE, by Entellus Medical, Inc.

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510(K) Number: K110739
Device Name: ENTELLUS MEDICAL SINUS GUIDEWIRE
Manufacturer: Entellus Medical, Inc.
Device Classification Name: instrument, ent manual surgical
Regulation Number: 874.4420
Classification Product Code: LRC
Date Received: 03/17/2011
Decision Date: 06/14/2011
Regulation Medical Specialty: Ear Nose & Throat
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