FDA 510(k), K992832, SULZER VASCUTEK EPTFE VASCULAR PROSTHESIS
FDA 510(k), K992832, SULZER VASCUTEK EPTFE VASCULAR PROSTHESIS
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510(K) Number: K992832
Device Name: SULZER VASCUTEK EPTFE VASCULAR PROSTHESIS
Manufacturer:
Device Classification Name: Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
Regulation Number: 870.3450
Classification Product Code: DSY
Date Received: 08/23/1999
Decision Date: 11/19/1999
Regulation Medical Specialty: Cardiovascular
Device Name: SULZER VASCUTEK EPTFE VASCULAR PROSTHESIS
Manufacturer:
Device Classification Name: Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
Regulation Number: 870.3450
Classification Product Code: DSY
Date Received: 08/23/1999
Decision Date: 11/19/1999
Regulation Medical Specialty: Cardiovascular