FDA product code · Clinical chemistry
Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems
9 FDA decisions since 2020. 510(k) reviews decided 2021–2025 took a median of 226 days (half between 148 and 291). 5 recalls name this code, 4 of them Class I. The most-cited predicate is K193371, named by 3 later devices.
An integrated continuous glucose monitoring system for replacement of finger stick blood glucose testing for diabetes treatment decisions in persons with diabetes, unless otherwise indicated. The system automatically measures glucose in bodily fluids continuously or frequently for a specified period of time. The system is also designed to reliably and securely transmit glucose measurement data to digitally…
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of QLG 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.
FDA decisions per year · QLG
2in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · QLG
259in 2021
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QLG
4in 2025
Class I (4 since 2007) Class II/III not classified
Adverse event reports per year · QLG
20,199in 2025
MAUDE reports naming product code QLG, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 1 | — | 0 | 1,069 |
| 2021 | 4 | 259 | 0 | 22,500 |
| 2022 | 2 | — | 0 | 26,528 |
| 2023 | 2 | — | 1 | 39,321 |
| 2024 | 0 | — | 0 | 35,108 |
| 2025 | 0 | — | 4 (4) | 20,199 |
| 2026 | 0 | — | 0 | — |
Planning a device in QLG? 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) ReportRelated product codes
Other codes under 21 CFR 862.1355.