ClearanceBrief
510(k) K830406 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

NON-STERILE CATHETER REPAIR KITS

ApplicantEvermed, Inc., Walker MI, US
DecisionSubstantially Equivalent, Mar 1, 1983
ReceivedFeb 7, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830406

DateFirm and productCodeLinked 510(k)
Feb 1, 2023Bard Peripheral Vascular Inc
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter Repair Kit 0601620 6.6F Broviac CV Catheter Repair Kit 0601630 9.6F Hickman CV Ca
Open, Classified
LJSNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.