Last synced on 25 January 2026 at 3:41 am

ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080806
510(k) Type
Traditional
Applicant
Possis Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2008
Days to Decision
14 days
Submission Type
Summary

ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080806
510(k) Type
Traditional
Applicant
Possis Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/4/2008
Days to Decision
14 days
Submission Type
Summary