510(k) K172772
K172772 is an FDA 510(k) premarket notification submitted by Dao Health for the device "Freemie Independence, Freemie Liberty". The FDA issued a decision of Substantially Equivalent on Oct 13, 2017. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Dao Health has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 13, 2017
- Date Received
- Sep 14, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Pump, Breast, Powered
- Device Class
- Class II
- Regulation Number
- 884.5160
- Review Panel
- OB
- Submission Type
- 510(k)