VICON

System, Optical Position/movement Recording

OXFORD MEDILOG, INC.

The following data is part of a premarket notification filed by Oxford Medilog, Inc. with the FDA for Vicon.

Pre-market Notification Details

• Device ID: K811172
• 510k Number: K811172
• Device Name: VICON
• Classification: System, Optical Position/movement Recording
• Applicant: OXFORD MEDILOG, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: LXJ
• CFR Regulation Number: 890.5360 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1981-04-28
• Decision Date: 1981-06-16

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
B548VICONVEROSYSTEM0	K811172	000
B548VICONVANTAGESYSTEM0	K811172	000
B548VICONTSERIESSYSTEM0	K811172	000
B548BONITASYSTEM0	K811172	000