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Radioassay, Triiodothyronine Uptake

FDA product code KHQ · Class 2 · Clinical Chemistry

28
Registered devices
4
Adverse events
1
Recalls
93
510(k) clearances

Devices with this code

Alinity — Abbott Ireland DiagnosticsT3 Uptake 125I RIA Kit — MP BIOMEDICALS, LLCT3 Uptake 125I RIA 200 Tube Kit — MP BIOMEDICALS, LLCVITROS — ORTHO CLINICAL DIAGNOSTICSTUptake — Roche Diagnostics GmbHiFlash-FT3 — Shenzhen YHLO Biotech Co., Ltd.ARCHITECT — ABBOTT LABORATORIEST3 Uptake AccuBind ELISA Test System - 192 Wells — MONOBIND, INC.ARCHITECT — ABBOTT LABORATORIESST AIA-PACK T-U — TOSOH CORPORATIONCEDIA T Uptake — Microgenics CorporationT3 Uptake AccuLite CLIA Test System - 192 Wells — MONOBIND, INC.T3 Uptake AccuBind ELISA Test System - 96 Wells — MONOBIND, INC.Dimension Vista® Flex® reagent cartridge TU — Siemens Healthcare Diagnostics Inc.T3-Uptake ELISA — DRG Instruments Gesellschaft mit beschränkter HaftungAtellica IM Tup — Siemens Healthcare Diagnostics Inc.Dimension® Flex® reagent cartridge TU — Siemens Healthcare Diagnostics Inc.T3-Uptake ELISA — DRG International IncDRI T-Uptake Calibrator Kit — Microgenics CorporationADVIA Centaur® Tup — Siemens Healthcare Diagnostics Inc.DRI T-Uptake — Microgenics CorporationVITROS — ORTHO CLINICAL DIAGNOSTICSADVIA Centaur® Tup — Siemens Healthcare Diagnostics Inc.Elecsys T-Uptake — Roche Diagnostics GmbH

Recent recalls

DateFirmReason
2018-03-05Tosoh Bioscience IncAsfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, dependin

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.