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LITHICRON MODEL 3-70C-B PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K771538
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1977
Days to Decision
11 days

LITHICRON MODEL 3-70C-B PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K771538
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/22/1977
Days to Decision
11 days