510(k) K170982
K170982 is an FDA 510(k) premarket notification submitted by Smiths Medical Ads, Inc. for the device "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)". The FDA issued a decision of Substantially Equivalent on August 24, 2017. The device falls under product code MEA (Pump, Infusion, Pca), a Class II device regulated under 21 CFR 880.5725. Smiths Medical Ads, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 2017
- Date Received
- April 3, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Infusion, Pca
- Device Class
- Class II
- Regulation Number
- 880.5725
- Review Panel
- HO
- Submission Type