Last synced on 14 November 2025 at 11:06 pm

JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K020784
510(k) Type
Traditional
Applicant
JOSTRA AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2003
Days to Decision
304 days
Submission Type
Summary

JOSTRA SINGLE STAGE VENOUS RETURN CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K020784
510(k) Type
Traditional
Applicant
JOSTRA AG
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2003
Days to Decision
304 days
Submission Type
Summary