Last synced on 14 November 2025 at 11:06 pm

ANGIOJET SOLENT DISTA THROMBECTOMY SET

Page Type
Cleared 510(K)
510(k) Number
K113363
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2012
Days to Decision
204 days
Submission Type
Summary

ANGIOJET SOLENT DISTA THROMBECTOMY SET

Page Type
Cleared 510(K)
510(k) Number
K113363
510(k) Type
Traditional
Applicant
MEDRAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2012
Days to Decision
204 days
Submission Type
Summary