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9.5 FRENCH PERCUTANEOUS DOUBLE LUMEN BALLOON

Page Type
Cleared 510(K)
510(k) Number
K882508
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1989
Days to Decision
276 days

9.5 FRENCH PERCUTANEOUS DOUBLE LUMEN BALLOON

Page Type
Cleared 510(K)
510(k) Number
K882508
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1989
Days to Decision
276 days