510(k) Report

510(k) · Cleared

Cleared

Suction Pump

K140031510(k) TraditionalCleared Apr 28, 2014112-day reviewClass II21 CFR 878.4780

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

Ding Hwa Co., Ltd. · JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

Cleared on Apr 28, 2014 as substantially equivalent to K112421 (Emg Technology Co., Ltd., 2011) after a 112-day review. Its family tree reaches back 3 generations to 1995.

Decided
Apr 28, 2014
Review
112 days
Class
Class II
Product code
JCX
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K944399 (1995). No later device cites it as a predicate yet.

  1. Root · 3 generations backK944399 Medi-PumpThomas Industries · 1995
  2. 2 generations backK041199 Medi-Pump Aspirator, Model 1615Thomas Industries · 2004
  3. 1 generation backK112421 Emg Suction UnitEmg Technology Co., Ltd. · 2011
  4. This deviceK140031 Suction PumpDing Hwa Co., Ltd. · 2014
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K944399Medi-PumpThomas Industries1995—
−2K041199Medi-Pump Aspirator, Model 1615Thomas Industries2004—
−1K112421Emg Suction UnitEmg Technology Co., Ltd.2011—
0 (this device)K140031Suction PumpDing Hwa Co., Ltd.2014—
FIG. 1 — Lineage of K140031, 1995–2014Source: 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), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JCX? 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 JCX device

  1. #1 K250964 Protable Phlegm Suction Unit (JMA D01)score 12.2 · 4 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? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K112421Emg Suction Unit
Summary page 1
…equivalent in all specifications and performance compared to the predicate device identified in K112421 and do not raise any new types of safety and effectiveness issues when compared to…
Emg Technology Co., Ltd.2011—

Also cleared against K112421: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • The line of descent spans 19 years and passes through 3 companies; a new generation was cleared every 7.2 years on median.
  • None of the 3 ancestors has a recall.
  • 1 other device also cites its predicate K112421.

How does its category compare?

All JCX devices

JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · JCX

2in 2025

2008: 42009: 12010: 12011: 22012: 22013: 52014: 42016: 22017: 22018: 22019: 32022: 12023: 12024: 12025: 22026 (partial year): 1
2007high 5 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JCX

30in 2019

2008: 43 days median2013: 144 days median2014: 106 days median2019: 30 days median
2007high 144 (2013) · low 30 (2019)2026

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

Recalls per year · JCX

1in 2020

2008: 32011: 22013: 22017: 12020: 12026 (partial year): 1
2007high 3 (2008) · low 0 (2007)2026

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

Adverse event reports per year · JCX

45in 2025

2007: 482008: 572009: 342010: 72011: 92012: 182013: 122014: 682015: 1182016: 1192017: 1022018: 1702019: 1322020: 892021: 2272022: 2152023: 1872024: 1032025: 45
2007high 227 (2021) · low 7 (2010)2025

MAUDE reports naming product code JCX, 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
20070—048
2008443357
20091—034
20101—07
20112—29
20122—018
20135144212
20144106068
20150—0118
20162—0119
20172—1102
20182—0170
20193300132
20200—189
20210—0227
20221—0215
20231—0187
20241—0103
20252—045
20261—1—

What is it indicated for?

AS-XXXX Suction Pump is intended to be used to remove bodily fluids from a patient's airway or respiratory system.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K140031: Suction Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140031

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026