FDA 510(k), K000281, WALLSTENT ENTERNAL PROSTHESIS
FDA 510(k), K000281, WALLSTENT ENTERNAL PROSTHESIS
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510(K) Number: K000281
Device Name: WALLSTENT ENTERNAL PROSTHESIS
Manufacturer:
Device Classification Name: Stent, Colonic, Metallic, Expandable
Regulation Number: 878.3610
Classification Product Code: MQR
Date Received: 01/31/2000
Decision Date: 05/12/2000
Regulation Medical Specialty: General & Plastic Surgery
Device Name: WALLSTENT ENTERNAL PROSTHESIS
Manufacturer:
Device Classification Name: Stent, Colonic, Metallic, Expandable
Regulation Number: 878.3610
Classification Product Code: MQR
Date Received: 01/31/2000
Decision Date: 05/12/2000
Regulation Medical Specialty: General & Plastic Surgery