FDA 510(k), K042172, CLEO 90 INFUSION SET

FDA 510(k), K042172, CLEO 90 INFUSION SET

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510(K) Number: K042172
Device Name: CLEO 90 INFUSION SET
Manufacturer: SMITHS MEDICAL MD, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 08/11/2004
Decision Date: 10/07/2004
Regulation Medical Specialty: General Hospital
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