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SIRECUST 400 SYSTEM PATIENT MONITORING

Page Type
Cleared 510(K)
510(k) Number
K802113
510(k) Type
Traditional
Applicant
ANALOGIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1981
Days to Decision
141 days

SIRECUST 400 SYSTEM PATIENT MONITORING

Page Type
Cleared 510(K)
510(k) Number
K802113
510(k) Type
Traditional
Applicant
ANALOGIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1981
Days to Decision
141 days