FDA 510(k) Applications for Medical Device Product Code "DWQ"
(Stripper, Vein, External)

FDA 510(k) Number Applicant Device Name Decision Date
K212894 LeMaitre Vascular Inc. PhasTIPP 03/31/2022
K041453 SMITH & NEPHEW, INC. SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 07/22/2004
K032387 SMITH & NEPHEW, INC. TRIVEX SYSTEM 10/29/2003


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