510(k) K212773
K212773 is an FDA 510(k) premarket notification submitted by Ardo Medical AG for the device "ARDO Alyssa". The FDA issued a decision of Substantially Equivalent on Apr 15, 2022. 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
- Apr 15, 2022
- Date Received
- Aug 31, 2021
- Clearance Type
- Traditional
- 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)