Last synced on 25 January 2026 at 3:41 am

EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS CF26000.CF29000,CF32000,CF35000,CF4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022071
510(k) Type
Traditional
Applicant
Embol-X, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2003
Days to Decision
233 days
Submission Type
Summary

EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS CF26000.CF29000,CF32000,CF35000,CF4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K022071
510(k) Type
Traditional
Applicant
Embol-X, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2003
Days to Decision
233 days
Submission Type
Summary