510(k) K173138
K173138 is an FDA 510(k) premarket notification submitted by Biim Ultrasound AS for the device "Biim Diagnostic Ultrasound System". The FDA issued a decision of Substantially Equivalent on Oct 27, 2017. The device falls under product code IYO (System, Imaging, Pulsed Echo, Ultrasonic), a Class II device regulated under 21 CFR 892.1560.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 27, 2017
- Date Received
- Sep 29, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Imaging, Pulsed Echo, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1560
- Review Panel
- RA
- Submission Type
- 510(k)