ClearanceBrief
510(k) K851058 ยท LDR Controller, Infusion, Intravascular, Electronic

DOSI FLOW

ApplicantLeventon, S.A., Barcelona, ES
DecisionSubstantially Equivalent, Apr 29, 1985
ReceivedMar 14, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851058

DateFirm and productCodeLinked 510(k)
Jun 21, 2011Leventon S. A. U.
"***DOSI-FLOW 1 I.V. EXTENSION SET WITH I.V. FLOW REGULATOR REGULADOR DE CAUDAL PARA SETS DE INFUSION I.V.***REF 259-0250***50 UNITS***STERILE OE***LATEX-FREE***LEVENTON LEVENTON, S.A.U. C/Newton, 18-
Terminated
LDRNone listed

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