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Handheld Pulse Oximeter

Page Type
Cleared 510(K)
510(k) Number
K213431
510(k) Type
Traditional
Applicant
Shenzhen Witleaf Medical Electronics Co.,Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/26/2023
Days to Decision
493 days
Submission Type
Summary

Handheld Pulse Oximeter

Page Type
Cleared 510(K)
510(k) Number
K213431
510(k) Type
Traditional
Applicant
Shenzhen Witleaf Medical Electronics Co.,Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/26/2023
Days to Decision
493 days
Submission Type
Summary