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MINIMON 7132B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K882198
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1988
Days to Decision
64 days

MINIMON 7132B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K882198
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1988
Days to Decision
64 days