Vascular Solutions, Inc.

Vascular Solutions, Inc. holds 103 FDA 510(k) medical device clearances, first cleared 2002, most recent 2018, with 17 FDA device recalls on record.

Clearances by Vascular Solutions, Inc. — page 2

101–103 of 103

K032204 — MODIFICATION TO VASCULAR SOLUTIONS VARI-LASE ENDOVENOUS LASER PROCEDURE KITCode GEX·2003-08-20
K030654 — VASCULAR SOLUTIONS VARI-LASE ENDOVENOUS LASER PROCEDURE KITCode GEX·2003-06-18
K012293 — VASCULAR SOLUTIONS DUETT FLOWABLE HEMOSTATCode QSX·2002-01-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.