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SOLEX CATHETER, MODEL SL2593

Page Type
Cleared 510(K)
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)
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