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BETATRON IV SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K872774
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1988
Days to Decision
175 days

BETATRON IV SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K872774
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/1988
Days to Decision
175 days