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PATHFINDER II ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K990173
510(k) Type
Traditional
Applicant
MAXXIM MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1999
Days to Decision
336 days
Submission Type
Summary

PATHFINDER II ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K990173
510(k) Type
Traditional
Applicant
MAXXIM MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1999
Days to Decision
336 days
Submission Type
Summary