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INTRA. OX HANDHELD TISSUE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K133983
510(k) Type
Traditional
Applicant
VIOPTIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2014
Days to Decision
259 days
Submission Type
Summary

INTRA. OX HANDHELD TISSUE OXIMETER

Page Type
Cleared 510(K)
510(k) Number
K133983
510(k) Type
Traditional
Applicant
VIOPTIX INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2014
Days to Decision
259 days
Submission Type
Summary