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CORDIS 13F CATHETER SHEATH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K000753
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2000
Days to Decision
29 days
Submission Type
Summary

CORDIS 13F CATHETER SHEATH INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K000753
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2000
Days to Decision
29 days
Submission Type
Summary