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CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023907
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2002
Days to Decision
23 days
Submission Type
Summary

CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023907
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2002
Days to Decision
23 days
Submission Type
Summary