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9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON

Page Type
Cleared 510(K)
510(k) Number
K892222
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1990
Days to Decision
529 days

9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON

Page Type
Cleared 510(K)
510(k) Number
K892222
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1990
Days to Decision
529 days