Last synced on 14 November 2025 at 11:06 pm

SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA

Page Type
Cleared 510(K)
510(k) Number
K894460
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1989
Days to Decision
76 days

SIEMENS SIRECUST 730, PATIENT MONITOR W/ARRHYTHMIA

Page Type
Cleared 510(K)
510(k) Number
K894460
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/1989
Days to Decision
76 days