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CYBERLITH IMPLANTABLE PULSE GEN. #253-02

Page Type
Cleared 510(K)
510(k) Number
K800644
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1980
Days to Decision
23 days

CYBERLITH IMPLANTABLE PULSE GEN. #253-02

Page Type
Cleared 510(K)
510(k) Number
K800644
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/1980
Days to Decision
23 days