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9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)

Page Type
Cleared 510(K)
510(k) Number
K903344
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1991
Days to Decision
174 days

9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)

Page Type
Cleared 510(K)
510(k) Number
K903344
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1991
Days to Decision
174 days