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Tempus Pro Patient Monitor

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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