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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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