FDA 510(k) Applications Submitted by ViOptix, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K090679 03/16/2009 VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM VIOPTIX, INC.
K141234 05/13/2014 ODISSEY TISSUE OXIMETER VIOPTIX, INC.
K042657 09/28/2004 VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2 VIOPTIX, INC.
K163472 12/12/2016 Intra.Ox Handheld Tissue Oximeter VIOPTIX, INC.
K221010 04/05/2022 Intra.Ox 2.0 Handheld Tissue Oximeter ViOptix, Inc.
K191676 06/24/2019 Intra.Ox 2.0 Handheld Tissue Oximeter ViOptix, Inc.


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