FDA product code · Clinical toxicology

Mercury, Atomic Absorption

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

DPHClass I21 CFR 862.3600510(k) required2 decisions since 19780 recalls

2 FDA decisions since 1978. 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 DPH 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 · DPH

FDA has decided no DPH device since 2007.

Median 510(k) review, days · DPH

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

Recalls per year · DPH

No recall names DPH since 2007.

Adverse event reports per year · DPH

No MAUDE report names DPH 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 — DPH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in DPH? 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

Mercury, Atomic Absorption

What has FDA decided in DPH lately?