Last synced on 18 April 2025 at 11:05 pm

CORDIS M3 PTA DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003920
510(k) Type
Abbreviated
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
178 days
Submission Type
Summary

CORDIS M3 PTA DILATATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003920
510(k) Type
Abbreviated
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/15/2001
Days to Decision
178 days
Submission Type
Summary