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PULSE GENERATOR MODEL 61 AND 128

Page Type
Cleared 510(K)
510(k) Number
K790562
510(k) Type
Traditional
Applicant
ELA MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1979
Days to Decision
50 days

PULSE GENERATOR MODEL 61 AND 128

Page Type
Cleared 510(K)
510(k) Number
K790562
510(k) Type
Traditional
Applicant
ELA MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1979
Days to Decision
50 days