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IMPLANTABLE PULSE GENERATOR PACEMAKER

Page Type
Cleared 510(K)
510(k) Number
K791417
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1979
Days to Decision
39 days

IMPLANTABLE PULSE GENERATOR PACEMAKER

Page Type
Cleared 510(K)
510(k) Number
K791417
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1979
Days to Decision
39 days