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VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200812
510(k) Type
Traditional
Applicant
Philips Image Guided Therapy Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2020
Days to Decision
159 days
Submission Type
Summary

VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K200812
510(k) Type
Traditional
Applicant
Philips Image Guided Therapy Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2020
Days to Decision
159 days
Submission Type
Summary