ClearanceBrief
510(k) K160457 ยท PEN Gram-Negative Bacteria And Associated Resistance Markers

FilmArray Blood Culture Identification (BCID) panel for use with FilmArray Torch

ApplicantBiofire Diagnostics, LLC, Salt Lake City UT, US
DecisionSubstantially Equivalent, Mar 15, 2016
ReceivedFeb 19, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K160457

DateFirm and productCodeLinked 510(k)
Jan 22, 2020BioFire Diagnostics, LLC
FilmArray BCID Panel, RFIT-ASY-0126, 30, Rx Only, CE, IVD, UDI: 00815381020086 used with the following BACT/ALERT Blood Culture Bottle Catalog No./Description: 410851/BACT/ALERT FA Plus 410852/BA
Terminated
PENNone listed
Jan 22, 2020BioFire Diagnostics, LLC
FilmArray BCID Panel, RFIT-ASY-0127, 6, Rx Only, CE, IVD, UDI: 00815381020093 used with the following BACT/ALERT Blood Culture Bottle Catalog No./Description: 410851/BACT/ALERT FA Plus 410852/BAC
Terminated
PENNone listed
Mar 7, 2019BioFire Diagnostics, LLC
FilmArray BCID Panel, IVD, Rx Only, BioFire Diagnostics, REF: RFIT-ASY-0126, and RFIT-ASY-0127, when used with the following blood culture bottles: Bottle Description/Part Number: BACT/ALERT FA Plus/4
Terminated
PENNone listed
Oct 30, 2018BioFire Diagnostics, LLC
FilmArray Blood Culture Identification (BCID), IVD, Rx Only, BioFire Diagnostics, LLC, Panel Catalog Numbers/ UDI: RFIT-ASY-0126 (30 test kit)/ 00815381020086, RFIT-ASY-0127 (6 test kit)/ 00815381020
Terminated
PAMNone listed
Apr 25, 2018BioFire Diagnostics, LLC
FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catal
Terminated
PENNone listed

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