DANA

Recorder, Attention Task Performance

ANTHROTRONIX, INC

The following data is part of a premarket notification filed by Anthrotronix, Inc with the FDA for Dana.

Pre-market Notification Details

• Device ID: K141865
• 510k Number: K141865
• Device Name: DANA
• Classification: Recorder, Attention Task Performance
• Applicant: ANTHROTRONIX, INC 8737 COLESVILLE ROAD SUITE L-203 Silver Spring, MD 20910
• Contact: Corina E Lathan, Phd, Pe
• Correspondent: Corina E Lathan, Phd, Pe; ANTHROTRONIX, INC 8737 COLESVILLE ROAD SUITE L-203 Silver Spring, MD 20910
• 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: 2014-07-10
• Decision Date: 2014-10-15
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00860011042105	K141865	000