510(k) Report

510(k) · Cleared

Cleared

Electric Breast Pump

K211024510(k) TraditionalCleared Feb 11, 2022311-day reviewClass II21 CFR 884.5160

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

Shantou Huihengqi Electronic Technology Co., Ltd. · HGX Pump, Breast, Powered

Cleared on Feb 11, 2022 as substantially equivalent to K201903 (Cixi Ruihong Electric Appliance Co., Ltd., 2021) after a 311-day review. Its family tree reaches back 7 generations to 1980. 3 later devices descend from it.

Decided
Feb 11, 2022
Review
311 days
Class
Class II
Product code
HGX
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K801862 (1980). 11 ancestors in all. 3 later devices descend from it, 3 citing it directly.

  1. Root · 7 generations backK801862 Medela Electric Breast PumpMedela, Inc. · 1980 · Recalled
  2. 6 generations backK020518 Medela Symphony Breast Pump, Model 024Medela, Inc. · 2002 · Recalled
  3. 5 generations backK053052 Medela Swing Breast PumpMedela AG · 2006
  4. 4 generations backK092783 DEBPEnko, Ltd. · 2009
  5. 3 generations backK162415 Spectra 9PlusUzinmedicare Company · 2017
  6. 2 generations backK163136 Youha electric breast pumpNingbo Youhe Electrical Appliance Technology Co., Ltd. · 2017
  7. 1 generation backK201903 Electric breast pump (Models: RH-228 and RH-338)Cixi Ruihong Electric Appliance Co., Ltd. · 2021
  8. This deviceK211024 Electric Breast PumpShantou Huihengqi Electronic Technology Co., Ltd. · 2022
  9. Descendant · cites it directly · 0 of its ownK252342 Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810)Guangdong Youmeng Electrical Technology Co., Ltd. · 2025
  10. Descendant · cites it directly · 0 of its ownK232477 Electric Breast Pump (Models AOV6818, AOV6821, AOV6826, AOV6830…Jiangxi AOV Maternity & Baby Products Co., Ltd. · 2024
  11. Descendant · cites it directly · 0 of its ownK233136 Hygeia Express Powered Breast PumpHygeia II Medical Group, Inc. · 2024

Most influential descendants

Showing 3 of 3 · See all
  • K252342Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810)Guangdong Youmeng Electrical Technology Co., Ltd. · 2025 · cites it directly0descendants
  • K232477Electric Breast Pump (Models AOV6818, AOV6821, AOV6826, AOV6830, AOV6852)Jiangxi AOV Maternity & Baby Products Co., Ltd. · 2024 · cites it directly0descendants
  • K233136Hygeia Express Powered Breast PumpHygeia II Medical Group, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K801862Medela Electric Breast PumpMedela, Inc.19801
−6K020518Medela Symphony Breast Pump, Model 024Medela, Inc.20023
−5K053052Medela Swing Breast PumpMedela AG2006—
−4K092783DEBPEnko, Ltd.2009—
−3K162415Spectra 9PlusUzinmedicare Company2017—
−2K163136Youha electric breast pumpNingbo Youhe Electrical Appliance Technology Co., Ltd.2017—
−1K201903Electric breast pump (Models: RH-228 and RH-338)Cixi Ruihong Electric Appliance Co., Ltd.2021—
0 (this device)K211024Electric Breast PumpShantou Huihengqi Electronic Technology Co., Ltd.2022—
+1K252342Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810)Guangdong Youmeng Electrical Technology Co., Ltd.2025—
+1K232477Electric Breast Pump (Models AOV6818, AOV6821, AOV6826, AOV6830, AOV6852)Jiangxi AOV Maternity & Baby Products Co., Ltd.2024—
+1K233136Hygeia Express Powered Breast PumpHygeia II Medical Group, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199010
199510
199710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202420
202510
FIG. 1 — Lineage of K211024, 1980–2025Source: 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 HGX? 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 HGX device

  1. #1 K212180 Wearable Breast Pump (Model S12)score 34.9 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K201903Electric breast pump (Models: RH-228 and RH-338)
Cleared while this submission was under review
Summary page 5
…wered Breast Pump Product Code: HGX; Classification: II Regulation Number: 21 CFR 884.5160 5. Identification of Predicate device 510(k) Number: K201903 Product Name: Electric breast pump (Models: RH-228 and RH-338) The predicate device has not been subject to a design-…
Cixi Ruihong Electric Appliance Co., Ltd.2021—

Also cleared against K201903: 3 other devices →

What descends from it? (3)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K252342Electric Breast Pump (YM-8807, YM-8805, YM-8806, YM-8810)Guangdong Youmeng Electrical Technology Co., Ltd.20250
K232477Electric Breast Pump (Models AOV6818, AOV6821, AOV6826, AOV6830, AOV6852)Jiangxi AOV Maternity & Baby Products Co., Ltd.20240
K233136Hygeia Express Powered Breast PumpHygeia II Medical Group, Inc.20240

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 42 years and passes through 7 companies; a new generation was cleared every 3.7 years on median.
  • 4 of the 11 ancestors have a recall of any class.
  • Of its descendants, K252342 (Guangdong Youmeng Electrical Technology Co., Ltd., 2025) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K201903.

How does its category compare?

All HGX devices

HGX Pump, Breast, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · HGX

34so far in 2026, the most since 2007

2007: 12008: 22009: 42010: 72011: 22012: 62013: 42014: 32015: 92016: 72017: 82018: 62019: 72020: 92021: 122022: 152023: 152024: 192025: 262026 (partial year): 34
2007high 34 (2026) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HGX

122in 2025

2009: 121 days median2010: 103 days median2012: 180 days median2013: 131 days median2014: 120 days median2015: 141 days median2016: 121 days median2017: 159 days median2018: 136 days median2019: 158 days median2020: 128 days median2021: 240 days median2022: 190 days median2023: 167 days median2024: 168 days median2025: 122 days median2026 (partial year): 142 days median
2007high 240 (2021) · low 103 (2010)2026

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

Recalls per year · HGX

1in 2017

2010: 52011: 12017: 1
2007high 5 (2010) · low 0 (2007)2026

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

Adverse event reports per year · HGX

69in 2025

2007: 22008: 22010: 882011: 2402012: 6852013: 8372014: 1,0362015: 4962016: 3732017: 4372018: 2912019: 1682020: 1682021: 1192022: 1542023: 2002024: 1182025: 69
2007high 1,036 (2014) · low 0 (2009)2025

MAUDE reports naming product code HGX, 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
20071—02
20082—02
2009412100
20107103588
20112—1240
201261800685
201341310837
2014312001,036
201591410496
201671210373
201781591437
201861360291
201971580168
202091280168
2021122400119
2022151900154
2023151670200
2024191680118
202526122069
2026341420—

What is it indicated for?

The Electric Breast Pump (Models 918, HF918) is a powered breast pump to be used by lactating women to express and collect milk from their breast. The Electric Breast Pump is intended for a single user.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K211024: Electric Breast Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K211024

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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