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Coag-Sense Prothrombin Time (PT) / INR Monitoring Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183255
510(k) Type
Traditional
Applicant
Coagusense, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2019
Days to Decision
92 days
Submission Type
Summary

Coag-Sense Prothrombin Time (PT) / INR Monitoring Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183255
510(k) Type
Traditional
Applicant
Coagusense, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2019
Days to Decision
92 days
Submission Type
Summary