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Intra.Ox Handheld Tissue Oximeter

Page Type
Cleared 510(K)
510(k) Number
K163472
510(k) Type
Traditional
Applicant
VIOPTIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2017
Days to Decision
339 days
Submission Type
Summary

Intra.Ox Handheld Tissue Oximeter

Page Type
Cleared 510(K)
510(k) Number
K163472
510(k) Type
Traditional
Applicant
VIOPTIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2017
Days to Decision
339 days
Submission Type
Summary