510(k) K214043
K214043 is an FDA 510(k) premarket notification submitted by Aidoc Medical , Ltd. for the device "BriefCase". The FDA issued a decision of Substantially Equivalent on Mar 14, 2022. The device falls under product code QFM (Radiological Computer-Assisted Prioritization Software For Lesions), a Class II device regulated under 21 CFR 892.2080. Aidoc Medical , Ltd. has 34 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 14, 2022
- Date Received
- Dec 23, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radiological Computer-Assisted Prioritization Software For Lesions
- Device Class
- Class II
- Regulation Number
- 892.2080
- Review Panel
- RA
- Submission Type
- 510(k)
Radiological computer-assisted prioritization software for lesions is an image processing device intended to aid in prioritization and triage of time sensitive patient detection and diagnosis based on the analysis of medical images acquired from radiological signal acquisition systems. The device identifies or prioritizes time sensitive imaging for review by prespecified clinical users based on software-based image analysis but does not provide information from the image analysis other than triage and notification.