FDA product code · Clinical chemistry

Copper Reduction, Glucose

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

CFWClass II21 CFR 862.1345510(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 chemistry panel

Twenty years of CFW 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 — CFW by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in CFW? 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 862.1345.

CGA Glucose Oxidase, Glucose LFR Glucose Dehydrogenase, Glucose PZI Prescription Use Blood Glucose Meter For…CGD Ferricyanide, Glucose CGE Orthotoluidine, Glucose NBW System, Test, Blood Glucose, Over The Counter MRV Drink, Glucose Tolerance PYV Hospital Continuous Glucose Monitoring System CFR Hexokinase, Glucose