Last synced on 25 January 2026 at 3:41 am

SOLEX CATHETER, MODEL SL2593

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081936
510(k) Type
Traditional
Applicant
Alsius Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2008
Days to Decision
37 days
Submission Type
Summary

SOLEX CATHETER, MODEL SL2593

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081936
510(k) Type
Traditional
Applicant
Alsius Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2008
Days to Decision
37 days
Submission Type
Summary