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JOSTRA DUAL STAGE VENOUS RETURN CANNULAE

Page Type
Cleared 510(K)
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)
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