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CYBERLITH I PULSE GENERATOR MODEL 253-04

Page Type
Cleared 510(K)
510(k) Number
K810385
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1981
Days to Decision
47 days

CYBERLITH I PULSE GENERATOR MODEL 253-04

Page Type
Cleared 510(K)
510(k) Number
K810385
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1981
Days to Decision
47 days