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FDA 510(k), K021362, LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
FDA 510(k), K021362, LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
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$149.00 USD
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$149.00 USD
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510(K) Number: K021362
Device Name: LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
Manufacturer: ORGAN RECOVERY SYSTEMS, INC.
Device Classification Name: system, perfusion, kidney
Regulation Number: 876.5880
Classification Product Code: KDN
Date Received: 04/30/2002
Decision Date: 07/31/2003
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
Manufacturer: ORGAN RECOVERY SYSTEMS, INC.
Device Classification Name: system, perfusion, kidney
Regulation Number: 876.5880
Classification Product Code: KDN
Date Received: 04/30/2002
Decision Date: 07/31/2003
Regulation Medical Specialty: Gastroenterology/Urology
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