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CORDIS 9 F GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K925131
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1993
Days to Decision
205 days
Submission Type
Summary

CORDIS 9 F GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K925131
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/1993
Days to Decision
205 days
Submission Type
Summary