Last synced on 25 January 2026 at 3:41 am

ACESSORY PACK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923638
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1993
Days to Decision
202 days
Submission Type
Summary

ACESSORY PACK

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K923638
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1993
Days to Decision
202 days
Submission Type
Summary