510(k) K150721
K150721 is an FDA 510(k) premarket notification submitted by Ardo Medical AG for the device "ARDO Calypso Pro Powered Breast Pump". The FDA issued a decision of Substantially Equivalent on Jun 17, 2015. 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
- Jun 17, 2015
- Date Received
- Mar 19, 2015
- 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)