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OVER THE WIRE EMBOLECTOMY CATHETER, MODEL 2302

Page Type
Cleared 510(K)
510(k) Number
K022145
510(k) Type
Traditional
Applicant
LEMAITRE VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2003
Days to Decision
196 days
Submission Type
Statement

OVER THE WIRE EMBOLECTOMY CATHETER, MODEL 2302

Page Type
Cleared 510(K)
510(k) Number
K022145
510(k) Type
Traditional
Applicant
LEMAITRE VASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2003
Days to Decision
196 days
Submission Type
Statement