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Leadtek Fingertip Pulse Oximeter

Page Type
Cleared 510(K)
510(k) Number
K193350
510(k) Type
Traditional
Applicant
Leadtek Research Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
4/27/2020
Days to Decision
146 days
Submission Type
Summary

Leadtek Fingertip Pulse Oximeter

Page Type
Cleared 510(K)
510(k) Number
K193350
510(k) Type
Traditional
Applicant
Leadtek Research Inc.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
4/27/2020
Days to Decision
146 days
Submission Type
Summary