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UNIPOLAR, ASYNCHRONOUS PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K770197
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1977
Days to Decision
7 days

UNIPOLAR, ASYNCHRONOUS PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K770197
510(k) Type
Traditional
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/1977
Days to Decision
7 days