510(k) K223347
K223347 is an FDA 510(k) premarket notification submitted by Ultrasight, Inc. for the device "UltraSight AI Guidance". The FDA issued a decision of Substantially Equivalent on Jul 24, 2023. The device falls under product code QJU (Image Acquisition And/Or Optimization Guided By Artificial Intelligence), a Class II device regulated under 21 CFR 892.2100. Ultrasight, Inc. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 24, 2023
- Date Received
- Nov 1, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Image Acquisition And/Or Optimization Guided By Artificial Intelligence
- Device Class
- Class II
- Regulation Number
- 892.2100
- Review Panel
- RA
- Submission Type
- 510(k)
A radiological acquisition and/or optimization guidance system is a device that is intended to aid in the acquisition and/or optimization of images and/or diagnostic signals. The device interfaces with the acquisition system, analyzes its output, and provides guidance and/or feedback to the operator for improving image and/or signal quality.