FDA product code · Cardiovascular

Phlebograph, Impedance

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

DQBClass II21 CFR 870.2750510(k) required3 decisions since 19770 recalls

3 FDA decisions since 1977. 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, cardiovascular panel

Twenty years of DQB 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 · DQB

FDA has decided no DQB device since 2007.

Median 510(k) review, days · DQB

Too few DQB 510(k)s in any year since 2007 to give a median.

Recalls per year · DQB

No recall names DQB since 2007.

Adverse event reports per year · DQB

No MAUDE report names DQB since 2007.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

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

Planning a device in DQB? 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

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What has FDA decided in DQB lately?

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