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MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872788
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1987
Days to Decision
73 days

MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872788
510(k) Type
Traditional
Applicant
URESIL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1987
Days to Decision
73 days