Last synced on 25 January 2026 at 3:41 am

MEDTRONIOC 7F LAUNCHER BIOPSY GUIDE CATHETER, MODEL LA7RVBB, MEDTRONIC 8F LAUNCHER BIOPSY CATHETER, MODEL LA8RVBB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030671
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2003
Days to Decision
150 days
Submission Type
Summary

MEDTRONIOC 7F LAUNCHER BIOPSY GUIDE CATHETER, MODEL LA7RVBB, MEDTRONIC 8F LAUNCHER BIOPSY CATHETER, MODEL LA8RVBB

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030671
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2003
Days to Decision
150 days
Submission Type
Summary