Last synced on 25 January 2026 at 3:41 am

ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101406
510(k) Type
Special
Applicant
Medrad Interventional/Possis
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2010
Days to Decision
28 days
Submission Type
Summary

ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101406
510(k) Type
Special
Applicant
Medrad Interventional/Possis
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2010
Days to Decision
28 days
Submission Type
Summary