FDA 510(k), K130357, SUPERDIMENSION TRIPLE-NEEDLE CYTOLOGY BRUSH

FDA 510(k), K130357, SUPERDIMENSION TRIPLE-NEEDLE CYTOLOGY BRUSH

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510(K) Number: K130357
Device Name: SUPERDIMENSION TRIPLE-NEEDLE CYTOLOGY BRUSH
Manufacturer:
Device Classification Name: Brush, Biopsy, Bronchoscope (Non-Rigid)
Regulation Number: 874.4680
Classification Product Code: BTG
Date Received: 02/13/2013
Decision Date: 11/06/2013
Regulation Medical Specialty: Ear Nose & Throat
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