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MODIFICATION TO 7F HYDROLYSER THROMBECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K990805
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1999
Days to Decision
4 days
Submission Type
Summary

MODIFICATION TO 7F HYDROLYSER THROMBECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K990805
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/1999
Days to Decision
4 days
Submission Type
Summary