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OSCOR PERMANENT RETRACTABLE SCREW-IN PACING LEAD MODEL PR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964107
510(k) Type
Traditional
Applicant
OSCOR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking & Post-Market Surveillance
Decision Date
4/1/1997
Days to Decision
168 days

OSCOR PERMANENT RETRACTABLE SCREW-IN PACING LEAD MODEL PR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964107
510(k) Type
Traditional
Applicant
OSCOR MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking & Post-Market Surveillance
Decision Date
4/1/1997
Days to Decision
168 days