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FDA 510(k), K113565, MULTI-MED CENTRAL VENOUS CATHETERS (CVCS), WITH AND WITHOUT HEPARIN VANTEX CENTRAL VENOUS CATHETERS (CVCS), WITH HEPARIN
FDA 510(k), K113565, MULTI-MED CENTRAL VENOUS CATHETERS (CVCS), WITH AND WITHOUT HEPARIN VANTEX CENTRAL VENOUS CATHETERS (CVCS), WITH HEPARIN
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510(K) Number: K113565
Device Name: MULTI-MED CENTRAL VENOUS CATHETERS (CVCS), WITH AND WITHOUT HEPARIN VANTEX CENTRAL VENOUS CATHETERS (CVCS), WITH HEPARIN
Manufacturer: EDWARDS LIFESCIENCES, LLC.
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 12/02/2011
Decision Date: 05/18/2012
Regulation Medical Specialty: General Hospital
Device Name: MULTI-MED CENTRAL VENOUS CATHETERS (CVCS), WITH AND WITHOUT HEPARIN VANTEX CENTRAL VENOUS CATHETERS (CVCS), WITH HEPARIN
Manufacturer: EDWARDS LIFESCIENCES, LLC.
Device Classification Name: catheter, intravascular, therapeutic, short-term less than 30 days
Regulation Number: 880.5200
Classification Product Code: FOZ
Date Received: 12/02/2011
Decision Date: 05/18/2012
Regulation Medical Specialty: General Hospital
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- Delivery: Approximately 1 to 2 weeks
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