510(k) Report

510(k) · Cleared

Cleared

Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62); Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62)

K261622510(k) TraditionalCleared Sep 3, 2026111-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

Philips Consumer Lifestyle B.V. · HGX Pump, Breast, Powered

Cleared on Sep 3, 2026 as substantially equivalent to K251377 (Medela AG, 2025) after a 111-day review. Its family tree reaches back 6 generations to 1980.

Decided
Sep 3, 2026
Review
111 days
Class
Class II
Product code
HGX
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K801862 (1980). 8 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 6 generations backK801862 Medela Electric Breast PumpMedela, Inc. · 1980 · Recalled
  2. 5 generations backK020518 Medela Symphony Breast Pump, Model 024Medela, Inc. · 2002 · Recalled
  3. 4 generations backK031614 Medela Pump in Style Advanced Breast PumpMedela, Inc. · 2003 · Recalled
  4. 3 generations backK181937 Pump In Style Advanced, Advanced Personal Double BreastpumpMedela, LLC · 2018
  5. 2 generations backK200508 Pump In StyleMedela, LLC · 2020
  6. 1 generation backK251377 Magic InBraMedela AG · 2025
  7. This deviceK261622 Philips Avent Natural Care Hands-free Wearable Electric Breast Pump…Philips Consumer Lifestyle B.V. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K801862Medela Electric Breast PumpMedela, Inc.19801
−5K020518Medela Symphony Breast Pump, Model 024Medela, Inc.20023
−4K031614Medela Pump in Style Advanced Breast PumpMedela, Inc.20031
−3K181937Pump In Style Advanced, Advanced Personal Double BreastpumpMedela, LLC2018—
−2K200508Pump In StyleMedela, LLC2020—
−1K251377Magic InBraMedela AG2025—
0 (this device)K261622Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model…Philips Consumer Lifestyle B.V.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199520
FIG. 1 — Lineage of K261622, 1980–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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
*K251377Magic InBra
Summary page 5
…Regulatory Class: Class II 5. Predicate Device Information Device Name: Magic InBra™ 510(k) Number: K251377 Manufacturer: Medela AG The predicate device has not been subject to a design-related recall. 6. Dev…
Medela AG2025—

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 46 years and passes through 4 companies; a new generation was cleared every 5.3 years on median.
  • 4 of the 8 ancestors have a recall of any class.

How does its category compare?

All HGX devices

HGX Pump, Breast, Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, 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 Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62) and the Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62) are powered breast pumps intended to express and collect milk from the breast of a lactating woman. The devices are intended for a single user.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K261622: Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62); Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K261622

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026