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KONTRON INTRA-AORTIC BALLOON PUMP MODEL K2000

Page Type
Cleared 510(K)
510(k) Number
K874816
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1988
Days to Decision
120 days

KONTRON INTRA-AORTIC BALLOON PUMP MODEL K2000

Page Type
Cleared 510(K)
510(k) Number
K874816
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1988
Days to Decision
120 days