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OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140286
510(k) Type
Special
Applicant
Cordis, A Johnson & Johnson Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2014
Days to Decision
30 days
Submission Type
Summary

OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140286
510(k) Type
Special
Applicant
Cordis, A Johnson & Johnson Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2014
Days to Decision
30 days
Submission Type
Summary