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ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192385
510(k) Type
Traditional
Applicant
ivWatch, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2020
Days to Decision
303 days
Submission Type
Summary

ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192385
510(k) Type
Traditional
Applicant
ivWatch, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2020
Days to Decision
303 days
Submission Type
Summary