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SIEMENS SIRECUST 730 PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K890791
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1989
Days to Decision
74 days

SIEMENS SIRECUST 730 PATIENT MONITOR

Page Type
Cleared 510(K)
510(k) Number
K890791
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/1989
Days to Decision
74 days