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MINIMON 7131B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K882197
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1988
Days to Decision
79 days

MINIMON 7131B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K882197
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1988
Days to Decision
79 days