510(k) · Cleared
ClearedModified Model UA-711 Digital Sphygmonometer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
A&D Engineering, Inc. · DSK Computer, Blood-Pressure
Cleared on Jun 24, 1987 after a 51-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 9 later devices descend from it.
- Decided
- Jun 24, 1987
- Review
- 51 days
- Class
- Class II
- Product code
- DSK
- Recalls
- None
- Predicates
- 0
9 later devices descend from it, 1 citing it directly.
- This deviceK871718 Modified Model UA-711 Digital SphygmonometerA&D Engineering, Inc. · 1987
- Descendant · cites it directly · 8 of its ownK032499 A & D Medical Lifesource UA-704 Digital Blood Pressure MonitorsA&D Engineering, Inc. · 2003
- Descendant · 2 generations on · 4 of its ownK061456 A & D Medical UM-101 Digital Blood Pressure MonitorA&D Engineering, Inc. · 2006
- Descendant · 3 generations on · 1 of its ownK173191 A&D Medical Blood Pressure MonitorsA&D Company, Ltd. · 2019
- Descendant · 2 generations on · 1 of its ownK083681 Bioland Blood Pressure MonitorBioland Technology, Ltd. · 2009
- Descendant · 4 generations on · 0 of its ownK212168 A&D Medical UM-212BLE Blood Pressure MonitorA&D Company, Ltd. · 2022
Showing 5 of 9 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 9 · See all- K032499A & D Medical Lifesource UA-704 Digital Blood Pressure MonitorsA&D Engineering, Inc. · 2003 · cites it directly8descendants
- K061456A & D Medical UM-101 Digital Blood Pressure MonitorA&D Engineering, Inc. · 2006 · 2 generations on4descendants
- K173191A&D Medical Blood Pressure MonitorsA&D Company, Ltd. · 2019 · 3 generations on1descendant
- K083681Bioland Blood Pressure MonitorBioland Technology, Ltd. · 2009 · 2 generations on1descendant
- K212168A&D Medical UM-212BLE Blood Pressure MonitorA&D Company, Ltd. · 2022 · 4 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K871718 | Modified Model UA-711 Digital Sphygmonometer | A&D Engineering, Inc. | 1987 | — |
| +1 | K032499 | A & D Medical Lifesource UA-704 Digital Blood Pressure Monitors | A&D Engineering, Inc. | 2003 | — |
| +2 | K061456 | A & D Medical UM-101 Digital Blood Pressure Monitor | A&D Engineering, Inc. | 2006 | — |
| +3 | K173191 | A&D Medical Blood Pressure Monitors | A&D Company, Ltd. | 2019 | — |
| +2 | K083681 | Bioland Blood Pressure Monitor | Bioland Technology, Ltd. | 2009 | — |
| +4 | K212168 | A&D Medical UM-212BLE Blood Pressure Monitor | A&D Company, Ltd. | 2022 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
| 2012 | 1 | 0 |
| 2019 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
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 DSK? 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 DSK device
- #1 K231586 Endophys Blood Pressure Monitor model BPM-30score 8.7 · 9 generations · no Class I recall
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? (9)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K032499 | A & D Medical Lifesource UA-704 Digital Blood Pressure Monitors | 2003 | 8 |
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, K032499 (A&D Engineering, Inc., 2003) has gone furthest, with 8 descendants of its own.
How does its category compare?
All DSK devicesDSK Computer, Blood-Pressure: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DSK
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · DSK
Too few DSK 510(k)s in any year since 2007 to give a median.
Recalls per year · DSK
No recall names DSK since 2007.
Adverse event reports per year · DSK
26in 2025
MAUDE reports naming product code DSK, 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 | 1 | — | 0 | 0 |
| 2008 | 1 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 10 |
| 2011 | 0 | — | 0 | 5 |
| 2012 | 0 | — | 0 | 69 |
| 2013 | 0 | — | 0 | 5 |
| 2014 | 0 | — | 0 | 8 |
| 2015 | 2 | — | 0 | 7 |
| 2016 | 1 | — | 0 | 13 |
| 2017 | 0 | — | 0 | 6 |
| 2018 | 0 | — | 0 | 93 |
| 2019 | 0 | — | 0 | 148 |
| 2020 | 0 | — | 0 | 29 |
| 2021 | 0 | — | 0 | 31 |
| 2022 | 0 | — | 0 | 29 |
| 2023 | 1 | — | 0 | 14 |
| 2024 | 0 | — | 0 | 12 |
| 2025 | 0 | — | 0 | 26 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K871718 · printed Nov 6, 2026
Cite this page
510(k) Report. “K871718: Modified Model UA-711 Digital Sphygmonometer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K871718
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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