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OPEN LOOP AMBULATORY INFUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K811774
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1981
Days to Decision
17 days

OPEN LOOP AMBULATORY INFUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K811774
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1981
Days to Decision
17 days