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CARDIAC PULSE GENERATOR, MODEL 160B

Page Type
Cleared 510(K)
510(k) Number
K780113
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1978
Days to Decision
25 days

CARDIAC PULSE GENERATOR, MODEL 160B

Page Type
Cleared 510(K)
510(k) Number
K780113
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1978
Days to Decision
25 days