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MINIMON 7136B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K883109
510(k) Type
Traditional
Applicant
KONTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1989
Days to Decision
176 days

MINIMON 7136B PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K883109
510(k) Type
Traditional
Applicant
KONTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1989
Days to Decision
176 days