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PATIENT MONITOR 575

Page Type
Cleared 510(K)
510(k) Number
K830433
510(k) Type
Traditional
Applicant
KONE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
43 days

PATIENT MONITOR 575

Page Type
Cleared 510(K)
510(k) Number
K830433
510(k) Type
Traditional
Applicant
KONE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/1983
Days to Decision
43 days