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Tempus Pro Patient Monitor

Page Type
Cleared 510(K)
510(k) Number
K173768
510(k) Type
Special
Applicant
Remote Diagnostic Technologies Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/10/2018
Days to Decision
30 days
Submission Type
Summary

Tempus Pro Patient Monitor

Page Type
Cleared 510(K)
510(k) Number
K173768
510(k) Type
Special
Applicant
Remote Diagnostic Technologies Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/10/2018
Days to Decision
30 days
Submission Type
Summary