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MINIMON 7133B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K896386
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1989
Days to Decision
37 days

MINIMON 7133B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K896386
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/1989
Days to Decision
37 days