FDA 510(k), K100577, ACCLARENT CYCLOPS MULTI-ANGLE ENDOSCOPE

FDA 510(k), K100577, ACCLARENT CYCLOPS MULTI-ANGLE ENDOSCOPE

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510(K) Number: K100577
Device Name: ACCLARENT CYCLOPS MULTI-ANGLE ENDOSCOPE
Manufacturer:
Device Classification Name: Nasopharyngoscope (Flexible Or Rigid)
Regulation Number: 874.4760
Classification Product Code: EOB
Date Received: 03/01/2010
Decision Date: 01/06/2011
Regulation Medical Specialty: Ear Nose & Throat
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