510(k) K201316
K201316 is an FDA 510(k) premarket notification submitted by Suzhou Peaksonic Medical Technology Co., Ltd. for the device "Bladder Scanner (Model: M3, M3-HD, M4, M4-HD)". The FDA issued a decision of Substantially Equivalent on Feb 26, 2021. The device falls under product code IYO (System, Imaging, Pulsed Echo, Ultrasonic), a Class II device regulated under 21 CFR 892.1560. Suzhou Peaksonic Medical Technology Co., Ltd. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 26, 2021
- Date Received
- May 18, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Imaging, Pulsed Echo, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1560
- Review Panel
- RA
- Submission Type
- 510(k)