510(k) K172059
K172059 is an FDA 510(k) premarket notification submitted by Linkquest, Inc. for the device "LinkQuest Diagnostic Ultrasound System model SQ860". The FDA issued a decision of Substantially Equivalent on Oct 5, 2017. 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
- Oct 5, 2017
- Date Received
- Jul 7, 2017
- 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
- 510(k)