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MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883265
510(k) Type
Traditional
Applicant
TELECTRONICS AND CORDIS PACING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1988
Days to Decision
74 days

MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883265
510(k) Type
Traditional
Applicant
TELECTRONICS AND CORDIS PACING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1988
Days to Decision
74 days