510(k) K260111
K260111 is an FDA 510(k) premarket notification submitted by Mytech Intelligence (Shenzhen) Co., Ltd. for the device "Palmtop Ultrasound Diagnostic System (MT10P/MT10)". The FDA issued a decision of Substantially Equivalent on May 14, 2026. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 14, 2026
- Date Received
- January 14, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Imaging, Pulsed Doppler, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1550
- Review Panel
- RA
- Submission Type