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KONTRON INTRA-AORTIC BALLOON PUMP MODEL K9000

Page Type
Cleared 510(K)
510(k) Number
K892878
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1989
Days to Decision
147 days

KONTRON INTRA-AORTIC BALLOON PUMP MODEL K9000

Page Type
Cleared 510(K)
510(k) Number
K892878
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1989
Days to Decision
147 days