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Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212779
510(k) Type
Special
Applicant
CoaguSense, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2022
Days to Decision
399 days
Submission Type
Summary

Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212779
510(k) Type
Special
Applicant
CoaguSense, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2022
Days to Decision
399 days
Submission Type
Summary