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GENERATOR, PULSE, UNIPOLAR, MODEL #504

Page Type
Cleared 510(K)
510(k) Number
K770716
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
8 days

GENERATOR, PULSE, UNIPOLAR, MODEL #504

Page Type
Cleared 510(K)
510(k) Number
K770716
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
8 days