Last synced on 25 January 2026 at 3:41 am

EMBOL-X ACCESS DEVICE/ AORTIC CANNULA, EMBOL-X SLIM ACCESSDEVICE/ AORTIC CANNULA, EMBOL-X GLIDE ACCESS DEVICE/ AORTIC CA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102420
510(k) Type
Special
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2010
Days to Decision
62 days
Submission Type
Summary

EMBOL-X ACCESS DEVICE/ AORTIC CANNULA, EMBOL-X SLIM ACCESSDEVICE/ AORTIC CANNULA, EMBOL-X GLIDE ACCESS DEVICE/ AORTIC CA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102420
510(k) Type
Special
Applicant
Edwards Lifesciences, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2010
Days to Decision
62 days
Submission Type
Summary