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FDA 510(k), K071538, ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER
FDA 510(k), K071538, ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER
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510(K) Number: K071538
Device Name: ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER
Manufacturer: ARROW INTERNATIONAL, INC.
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 06/05/2007
Decision Date: 08/30/2007
Regulation Medical Specialty: General Hospital
Device Name: ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER
Manufacturer: ARROW INTERNATIONAL, INC.
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 06/05/2007
Decision Date: 08/30/2007
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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