FDA 510(k), K011741, CRIT-LINE MONITOR III TQA (CLM TQA)

FDA 510(k), K011741, CRIT-LINE MONITOR III TQA (CLM TQA)

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510(K) Number: K011741
Device Name: CRIT-LINE MONITOR III TQA (CLM TQA)
Manufacturer:
Device Classification Name: System, Dialysate Delivery, Single Pass
Regulation Number: 876.5820
Classification Product Code: FIL
Date Received: 06/05/2001
Decision Date: 07/23/2002
Regulation Medical Specialty: Gastroenterology/Urology
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