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PULSE GENERATOR, LITKICRON MODEL 3-70H

Page Type
Cleared 510(K)
510(k) Number
K770507
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1977
Days to Decision
21 days

PULSE GENERATOR, LITKICRON MODEL 3-70H

Page Type
Cleared 510(K)
510(k) Number
K770507
510(k) Type
Traditional
Applicant
MEDCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/1977
Days to Decision
21 days