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CARDIAC PULSE GENERATOR, 16 SERIES

Page Type
Cleared 510(K)
510(k) Number
K790867
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1979
Days to Decision
24 days

CARDIAC PULSE GENERATOR, 16 SERIES

Page Type
Cleared 510(K)
510(k) Number
K790867
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/1979
Days to Decision
24 days