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7F HYDROLYSER THROMBECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K983534
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
140 days
Submission Type
Summary

7F HYDROLYSER THROMBECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K983534
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1999
Days to Decision
140 days
Submission Type
Summary