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EV1000 Clinical Platform with ClearSight Finger Cuff or ClearSight System, EV1000 Clinical Platform

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160552
510(k) Type
Traditional
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2016
Days to Decision
93 days
Submission Type
Summary

EV1000 Clinical Platform with ClearSight Finger Cuff or ClearSight System, EV1000 Clinical Platform

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160552
510(k) Type
Traditional
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2016
Days to Decision
93 days
Submission Type
Summary