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KONTRON VITALMON 5010 PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K852249
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1986
Days to Decision
511 days

KONTRON VITALMON 5010 PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K852249
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1986
Days to Decision
511 days