QBTEST

Recorder, Attention Task Performance

QBTECH AB

The following data is part of a premarket notification filed by Qbtech Ab with the FDA for Qbtest.

Pre-market Notification Details

• Device ID: K040894
• 510k Number: K040894
• Device Name: QBTEST
• Classification: Recorder, Attention Task Performance
• Applicant: QBTECH AB MIMERGATAN 5 Goteborg, SE 417 64
• Contact: Maria Berglund
• Correspondent: Maria Berglund; QBTECH AB MIMERGATAN 5 Goteborg, SE 417 64
• Product Code: LQD
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2004-04-06
• Decision Date: 2004-06-22
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
07350103930067	K040894	000