510(k) Report

510(k) · Cleared

Cleared

Electric Double Breast Pumps

K151284510(k) TraditionalCleared Dec 21, 2015221-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

Wuxi Xinzhongrui Baby Supplies Co., Ltd. · HGX Pump, Breast, Powered

Cleared on Dec 21, 2015 as substantially equivalent to K142479 (Wuxi Xinzhongrui Baby Supplies Co., Ltd., 2015) after a 221-day review. Its family tree reaches back 4 generations to 1988. 1 later device descends from it.

Decided
Dec 21, 2015
Review
221 days
Class
Class II
Product code
HGX
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K875300 (1988). 5 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK875300 Medela Breast-Pump LactinaMedela, Inc. · 1988 · Recalled
  2. 3 generations backK973501 Expresse and Premier Powered Breast PumpsAmeda Medizintechnik AG · 1997 · Recalled
  3. 2 generations backK113664 Closer to Nature Electric Breast PumpMayborn Group Limited · 2012
  4. 1 generation backK142479 Megna Breast PumpsWuxi Xinzhongrui Baby Supplies Co., Ltd. · 2015
  5. This deviceK151284 Electric Double Breast PumpsWuxi Xinzhongrui Baby Supplies Co., Ltd. · 2015
  6. Descendant · cites it directly · 0 of its ownK191802 Electric Breast PumpNingbo Huiyoo Baby Products Co., Ltd. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K191802Electric Breast PumpNingbo Huiyoo Baby Products Co., Ltd. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K875300Medela Breast-Pump LactinaMedela, Inc.19883
−3K973501Expresse and Premier Powered Breast PumpsAmeda Medizintechnik AG19971
−2K113664Closer to Nature Electric Breast PumpMayborn Group Limited2012—
−1K142479Megna Breast PumpsWuxi Xinzhongrui Baby Supplies Co., Ltd.2015—
0 (this device)K151284Electric Double Breast PumpsWuxi Xinzhongrui Baby Supplies Co., Ltd.2015—
+1K191802Electric Breast PumpNingbo Huiyoo Baby Products Co., Ltd.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K151284, 1988–2020Source: 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
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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
*K142479Megna Breast Pumps
Summary page 5
…1/3 5. Identification of Predicate Device 510(k) Number: K142479 Product Name: Megna Breast Pumps Model Name: M10 6. Substantially Equivalent (SE) Comparison…
Wuxi Xinzhongrui Baby Supplies Co., Ltd.2015—

Also cleared against K142479: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K191802Electric Breast PumpNingbo Huiyoo Baby Products Co., Ltd.20200

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 27 years and passes through 4 companies; a new generation was cleared every 9.7 years on median.
  • 2 of the 5 ancestors have a recall of any class.
  • Of its descendants, K191802 (Ningbo Huiyoo Baby Products Co., Ltd., 2020) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K142479.

How does its category compare?

All HGX devices

HGX Pump, Breast, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, 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 powered Electric Double Breast Pumps are intended to express and collect milk from the breast of a lactating woman.

They are double pumps with a single pumping option and intended for single user.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151284: Electric Double Breast Pumps.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151284

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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