510(k) K210124
K210124 is an FDA 510(k) premarket notification submitted by Uzinmedicare Co. for the device "Synergy Gold (SG) Portable (Models MM011450 and MM011460)". The FDA issued a decision of Substantially Equivalent on Oct 19, 2021. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Uzinmedicare Co. has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 19, 2021
- Date Received
- Jan 19, 2021
- 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)