FDA 510(k), K140382, AEROMINI TRACHEOBRONCHIAL STENT TECHNOLOGY

FDA 510(k), K140382, AEROMINI TRACHEOBRONCHIAL STENT TECHNOLOGY

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510(K) Number: K140382
Device Name: AEROMINI TRACHEOBRONCHIAL STENT TECHNOLOGY
Manufacturer:
Device Classification Name: Prosthesis, Tracheal, Expandable
Regulation Number: 878.3720
Classification Product Code: JCT
Date Received: 02/14/2014
Decision Date: 11/25/2014
Regulation Medical Specialty: General & Plastic Surgery
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