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IMPLANTED PACEMAKER PLUSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K771670
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1977
Days to Decision
11 days

IMPLANTED PACEMAKER PLUSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K771670
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1977
Days to Decision
11 days