Last synced on 25 April 2025 at 11:05 pm

EpiWatch Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243515
510(k) Type
Traditional
Applicant
EpiWatch, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2025
Days to Decision
114 days
Submission Type
Summary

EpiWatch Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243515
510(k) Type
Traditional
Applicant
EpiWatch, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2025
Days to Decision
114 days
Submission Type
Summary