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CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K034050
510(k) Type
Traditional
Applicant
Cordis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2004
Days to Decision
83 days
Submission Type
Summary

CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K034050
510(k) Type
Traditional
Applicant
Cordis Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2004
Days to Decision
83 days
Submission Type
Summary