ClearanceBrief
510(k) K093489 ยท FPA Set, Administration, Intravascular

IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGY

ApplicantRymed Technologies, Inc., Shelton CT, US
DecisionSubstantially Equivalent, Jul 29, 2010
ReceivedNov 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093489

DateFirm and productCodeLinked 510(k)
Jan 21, 2016Rymed Technologies, LLC
InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for single patient use in intravenous and blood administration sets without the need
Terminated
FPANone listed

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