Last synced on 9 May 2025 at 11:05 pm

CAROTID BALLOON SHUNT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860497
510(k) Type
Traditional
Applicant
IMODEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1986
Days to Decision
107 days

CAROTID BALLOON SHUNT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860497
510(k) Type
Traditional
Applicant
IMODEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/28/1986
Days to Decision
107 days