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CYBERLITH IX IMPLANTABLE PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K801337
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1981
Days to Decision
476 days

CYBERLITH IX IMPLANTABLE PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K801337
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1981
Days to Decision
476 days