Last synced on 14 November 2025 at 11:06 pm

ENDOHELIX ENDARTERECTOMY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K032105
510(k) Type
Traditional
Applicant
ENDARX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
114 days
Submission Type
Summary

ENDOHELIX ENDARTERECTOMY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K032105
510(k) Type
Traditional
Applicant
ENDARX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
114 days
Submission Type
Summary