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SIEMENS SIRECUST 732, PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K901771
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1990
Days to Decision
41 days

SIEMENS SIRECUST 732, PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K901771
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/1990
Days to Decision
41 days