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PULSE GENERATOR, IMPLANTABLE CARDIAC

Page Type
Cleared 510(K)
510(k) Number
K782149
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1979
Days to Decision
44 days

PULSE GENERATOR, IMPLANTABLE CARDIAC

Page Type
Cleared 510(K)
510(k) Number
K782149
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1979
Days to Decision
44 days