510(k) Report

FDA product code · Cardiovascular

Blood Pressure Cuff

DXQClass II21 CFR 870.1120510(k) required199 decisions since 197617 recalls

199 FDA decisions since 1976. 510(k) reviews decided 2021–2025 took a median of 97 days (half between 63 and 108). 17 recalls name this code, 0 of them Class I. The most-cited predicate is K974080, named by 9 later devices.

A blood pressure cuff is a device that has an inflatable bladder in an elastic sleeve (cuff) with a mechanism for inflating the bladder. The cuff is used to determine a subject's blood pressure.

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 DXQ 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 · DXQ

3in 2025

2007: 22008: 72009: 52010: 22011: 52012: 42013: 22014: 42015: 102016: 42017: 22018: 52019: 32020: 32021: 42022: 42023: 52024: 22025: 32026 (partial year): 4
2007high 10 (2015) · low 2 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DXQ

174in 2025

2008: 118 days median2009: 57 days median2011: 121 days median2012: 102 days median2014: 105 days median2015: 59 days median2016: 217 days median2018: 225 days median2019: 44 days median2020: 207 days median2021: 105 days median2022: 105 days median2023: 79 days median2025: 174 days median2026 (partial year): 102 days median
2007high 225 (2018) · low 44 (2019)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DXQ

1in 2025

2011: 12025: 1
2007high 1 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DXQ

20in 2025

2007: 32008: 42009: 22010: 12011: 52012: 72013: 92014: 92015: 232016: 502017: 672018: 442019: 412020: 52021: 122022: 32023: 202024: 152025: 20
2007high 67 (2017) · low 1 (2010)2025

MAUDE reports naming product code DXQ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—03
2008711804
200955702
20102—01
2011512115
2012410207
20132—09
2014410509
20151059023
20164217050
20172—067
20185225044
2019344041
2020320705
20214105012
2022410503
2023579020
20242—015
20253174120
202641020—
FIG. 1 — DXQ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in DXQ? 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 870.1120.