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PRONTO V3 EXTRACTION CENTER, MODEL 5003, PRONTO LP EXTRACTION CATHETER, MODEL 5010, SKYWAY RX SUPPORT CATHETER,

Page Type
Cleared 510(K)
510(k) Number
K083784
510(k) Type
Traditional
Applicant
VASCULAR SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2009
Days to Decision
101 days
Submission Type
Summary

PRONTO V3 EXTRACTION CENTER, MODEL 5003, PRONTO LP EXTRACTION CATHETER, MODEL 5010, SKYWAY RX SUPPORT CATHETER,

Page Type
Cleared 510(K)
510(k) Number
K083784
510(k) Type
Traditional
Applicant
VASCULAR SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/2009
Days to Decision
101 days
Submission Type
Summary