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PULSE GENERATOR MODEL 61 AND 128

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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