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PULSE GENERATOR, BIPOLAR, DEMAND

Page Type
Cleared 510(K)
510(k) Number
K772241
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1978
Days to Decision
53 days

PULSE GENERATOR, BIPOLAR, DEMAND

Page Type
Cleared 510(K)
510(k) Number
K772241
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1978
Days to Decision
53 days