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IMPLANTABLE PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K834096
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1983
Days to Decision
18 days

IMPLANTABLE PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K834096
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1983
Days to Decision
18 days