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LEMAITRE EMBOLECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992368
510(k) Type
Traditional
Applicant
VASCUTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
147 days
Submission Type
Statement

LEMAITRE EMBOLECTOMY CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992368
510(k) Type
Traditional
Applicant
VASCUTECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1999
Days to Decision
147 days
Submission Type
Statement