Last synced on 18 April 2025 at 11:05 pm

CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032737
510(k) Type
Special
Applicant
CORDIS EUROPA N.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2003
Days to Decision
28 days
Submission Type
Summary

CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032737
510(k) Type
Special
Applicant
CORDIS EUROPA N.V.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2003
Days to Decision
28 days
Submission Type
Summary