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MODIFIED BETATRON IV INSULIN INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K900498
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1990
Days to Decision
36 days

MODIFIED BETATRON IV INSULIN INFUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K900498
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/1990
Days to Decision
36 days