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CORDIS 7 FRENCH THRULUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K922891
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1993
Days to Decision
372 days
Submission Type
Summary

CORDIS 7 FRENCH THRULUMEN CATHETER

Page Type
Cleared 510(K)
510(k) Number
K922891
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1993
Days to Decision
372 days
Submission Type
Summary