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ADROIT GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K131225
510(k) Type
Special
Applicant
CORDIS CORP., A JOHNSON & JOHNSON CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2013
Days to Decision
29 days
Submission Type
Summary

ADROIT GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K131225
510(k) Type
Special
Applicant
CORDIS CORP., A JOHNSON & JOHNSON CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2013
Days to Decision
29 days
Submission Type
Summary