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MODIFICATION TO HYPERTRANSIT INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K070279
510(k) Type
Special
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2007
Days to Decision
44 days
Submission Type
Summary

MODIFICATION TO HYPERTRANSIT INFUSION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K070279
510(k) Type
Special
Applicant
CORDIS NEUROVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2007
Days to Decision
44 days
Submission Type
Summary