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: K180647
• 510k Number: K180647
• Device Name: BriefCase
• Classification: Radiological Computer-assisted Triage And Notification Software
• Applicant: Aidoc Medical, Ltd. Yigal Alon 92 Tel-aviv, IL 6789138
• Contact: Nimrod Epstein
• Correspondent: John J. Smith; Hogan Lovells US LLP 555 Thirteenth St. NW 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: 2018-03-12
• Decision Date: 2018-08-01
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
07290018052013	K180647	000