510(k) K172067
K172067 is an FDA 510(k) premarket notification submitted by Ardo Medical AG for the device "One Mum Pumpset". The FDA issued a decision of Substantially Equivalent on Nov 29, 2017. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Ardo Medical AG has 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 29, 2017
- Date Received
- Jul 7, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Breast, Powered
- Device Class
- Class II
- Regulation Number
- 884.5160
- Review Panel
- OB
- Submission Type
- 510(k)