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700-F SERIES STIMULATION ELECTRODES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964469
510(k) Type
Traditional
Applicant
Cardiotronics Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1996
Days to Decision
34 days
Submission Type
Statement

700-F SERIES STIMULATION ELECTRODES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964469
510(k) Type
Traditional
Applicant
Cardiotronics Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1996
Days to Decision
34 days
Submission Type
Statement