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JOSTRA DUAL STAGE VENOUS RETURN CANNULAE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013944
510(k) Type
Traditional
Applicant
JOSTRA AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2002
Days to Decision
74 days
Submission Type
Summary

JOSTRA DUAL STAGE VENOUS RETURN CANNULAE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013944
510(k) Type
Traditional
Applicant
JOSTRA AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2002
Days to Decision
74 days
Submission Type
Summary