FDA product code · Clinical toxicology

Radioimmunoassay, Morphine (3-H), Goat Antibody Ammonium Sulfate Sep.

Name: FDA decisions, review times, recalls and adverse event reports for product code DIQ
Creator: 510(k) Report

DIQClass II21 CFR 862.3640510(k) required0 decisions0 recalls

0 FDA decisions. No recall names this code.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, clinical toxicology panel

Twenty years of DIQ at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FIG. 1 — DIQ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in DIQ? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 862.3640.

DNK Thin Layer Chromatography, Morphine DMY Gas Chromatography, Morphine NGI Test, Morphine, Over The Counter DJJ Fluorometry, Morphine DOE Radioimmunoassay, Morphine (125-I), Goat…DNA Radioimmunoassay, Morphine-Barbiturate…PVG Test, Morphine, Employment And Insurance…DLR Hemagglutination Inhibition, Morphine DPK Liquid Chromatography, Morphine DOK Free Radical Assay, Morphine