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POSSIS ANGIOJET RAPID THROMBECTOMY CATHETER SYSTEM, F105 CATHETER,MODEL 3030C,LF140 CATHETER,MODEL 3040C,PUMP SET 3020P

Page Type
Cleared 510(K)
510(k) Number
K960970
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1996
Days to Decision
267 days
Submission Type
Summary

POSSIS ANGIOJET RAPID THROMBECTOMY CATHETER SYSTEM, F105 CATHETER,MODEL 3030C,LF140 CATHETER,MODEL 3040C,PUMP SET 3020P

Page Type
Cleared 510(K)
510(k) Number
K960970
510(k) Type
Traditional
Applicant
POSSIS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/3/1996
Days to Decision
267 days
Submission Type
Summary