BriefCase

Radiological Computer-assisted Triage And Notification Software

Aidoc Medical, Ltd.

The following data is part of a premarket notification filed by Aidoc Medical, Ltd. with the FDA for Briefcase.

Pre-market Notification Details

• Device ID: K222329
• 510k Number: K222329
• Device Name: BriefCase
• Classification: Radiological Computer-assisted Triage And Notification Software
• Applicant: Aidoc Medical, Ltd. 3 Aminadav St., Tel Aviv, IL 6706703
• Contact: Amalia Schreie
• Correspondent: John J Smith; Hogan Lovells US LLP 555 Thirteenth St Washington, DC 20004
• Product Code: QAS
• CFR Regulation Number: 892.2080 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2022-08-02
• Decision Date: 2022-09-28