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FDA 510(k), K170982, CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM)
FDA 510(k), K170982, CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM)
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510(K) Number: K170982
Device Name: CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM)
Manufacturer: Breanna Fautsch
Device Classification Name: Pump, Infusion, Pca
Regulation Number: MEA
Classification Product Code: KXA
Date Received: 04/03/2017
Decision Date: 08/24/2017
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM)
Manufacturer: Breanna Fautsch
Device Classification Name: Pump, Infusion, Pca
Regulation Number: MEA
Classification Product Code: KXA
Date Received: 04/03/2017
Decision Date: 08/24/2017
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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