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SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR

Page Type
Cleared 510(K)
510(k) Number
K863042
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1987
Days to Decision
155 days

SIRECUST 888/888R NON-INVASIVE BLOOD PRESS MONITOR

Page Type
Cleared 510(K)
510(k) Number
K863042
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/1987
Days to Decision
155 days