ClearanceBrief
510(k) K162911 ยท GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus

Sofia RSV FIA on Sofia 2 analyzer

ApplicantQuidel Corporation, San Diego, CA, US
DecisionSubstantially Equivalent, Feb 22, 2017
ReceivedOct 17, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K162911

DateFirm and productCodeLinked 510(k)
Dec 15, 2017Quidel Corporation
Sofia 2 Analyzer Catalog Number 20299 Sofia 2 is a bench top analyzer intended to be used with Cassette-based immunofluorescent in vitro diagnostic assays . Sofia 2 is intended for professional and
Terminated
PSZNone listed

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