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MODIFICATION TO EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032390
510(k) Type
Special
Applicant
EBI, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2003
Days to Decision
25 days
Submission Type
Summary

MODIFICATION TO EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032390
510(k) Type
Special
Applicant
EBI, L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/29/2003
Days to Decision
25 days
Submission Type
Summary