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Oxyfit Pulse Oximeter

Page Type
Cleared 510(K)
510(k) Number
K203812
510(k) Type
Traditional
Applicant
Shenzhen Viatom Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/8/2022
Days to Decision
680 days
Submission Type
Summary

Oxyfit Pulse Oximeter

Page Type
Cleared 510(K)
510(k) Number
K203812
510(k) Type
Traditional
Applicant
Shenzhen Viatom Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/8/2022
Days to Decision
680 days
Submission Type
Summary