510(k) Report

510(k) · Cleared

Cleared

Aneroid Type Blood Pressure Kit

K780715510(k) TraditionalCleared Jul 17, 197881-day reviewClass II21 CFR 870.1120

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Mars Metal Co., Ltd. · DXQ Blood Pressure Cuff

Cleared on Jul 17, 1978 after an 81-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jul 17, 1978
Review
81 days
Class
Class II
Product code
DXQ
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2019: 1 descendant cleared19801990200020102020
  1. This deviceK780715 Aneroid Type Blood Pressure KitMars Metal Co., Ltd. · 1978
  2. Descendant · cites it directly · 0 of its ownK191209 Aneroid Type Blood Pressure KitDongguan Mars Medical Products Co., Ltd. · 2019

Most influential descendants

Showing 1 of 1 · See all
  • K191209Aneroid Type Blood Pressure KitDongguan Mars Medical Products Co., Ltd. · 2019 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K780715Aneroid Type Blood Pressure KitMars Metal Co., Ltd.1978—
+1K191209Aneroid Type Blood Pressure KitDongguan Mars Medical Products Co., Ltd.2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
FIG. 1 — Lineage of K780715, 1978–2019Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DXQ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new DXQ device

  1. #1 K254287 Medline Reusable Blood Pressure Cuffscore 13.4 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K191209Aneroid Type Blood Pressure KitDongguan Mars Medical Products Co., Ltd.20190

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K191209 (Dongguan Mars Medical Products Co., Ltd., 2019) has gone furthest, with 0 descendants of its own.

How does its category compare?

All DXQ devices

DXQ Blood Pressure Cuff: FDA decisions, review times, recalls and adverse event reports over 20 years.

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—
Cite this page

510(k) Report. “K780715: Aneroid Type Blood Pressure Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K780715

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026