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ALERTWATCH: OR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130401
510(k) Type
Traditional
Applicant
Alertwatch, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2014
Days to Decision
353 days
Submission Type
Summary

ALERTWATCH: OR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130401
510(k) Type
Traditional
Applicant
Alertwatch, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2014
Days to Decision
353 days
Submission Type
Summary