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KONTRON CUTANEOUS PO2 MONITOR 820

Page Type
Cleared 510(K)
510(k) Number
K860951
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1986
Days to Decision
28 days

KONTRON CUTANEOUS PO2 MONITOR 820

Page Type
Cleared 510(K)
510(k) Number
K860951
510(k) Type
Traditional
Applicant
KONTRON INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/1986
Days to Decision
28 days