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510(k) K201381

Philips Avent Single/Double electric breast pump Advanced by Philips Consumer Lifestyle - Innovation Site Eindhoven — Product Code HGX

K201381 is an FDA 510(k) premarket notification submitted by Philips Consumer Lifestyle - Innovation Site Eindhoven for the device "Philips Avent Single/Double electric breast pump Advanced". The FDA issued a decision of Substantially Equivalent on Oct 1, 2020. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Philips Consumer Lifestyle - Innovation Site Eindhoven has 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Oct 1, 2020
Date Received
May 26, 2020
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Breast, Powered
Device Class
Class II
Regulation Number
884.5160
Review Panel
OB
Submission Type
510(k)

Other clearances by Philips Consumer Lifestyle - Innovation Site Eindhoven

  • K203383 — Philips Avent Double electric breast pump Advanced SCF394/61, Philips Avent… (Dec 15, 2020)
  • K161532 — Philips Avent Comfort Single/Twin Electric Breast Pump (Aug 29, 2016)

Other clearances for product code HGX

  • K254203 — Wearable Breast Pump (Model S36) (Sep 17, 2026)
  • K261622 — Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model… (Sep 3, 2026)
  • K262774 — Wearable breast pump (Model: XN/MD-2249BS, ZFHF) (Sep 1, 2026)
  • K260643 — Cimilre Dual Max (Aug 21, 2026)
  • K261298 — Wearable Electric Breast Pump (YM-8837, YM-8838, YM-8856(H03), YM-8809(S42)) (Aug 20, 2026)
  • K260259 — DiscreetDuo™ Flow Wearable Breast Pump (Model S3) (Jul 24, 2026)
  • K261199 — Wearable Breast Pump (Model S32A) (Jul 13, 2026)
  • K250070 — Electric breast pump (MY-375,MY-376,MY-378,MY-379,MY-380,V3) (Jun 26, 2026)
  • K261025 — Wearable breast pump (QY-101, QY-102, QY-108) (Jun 25, 2026)
  • K254254 — Momcozy Wearable Breast Pump (BP311, BP311-A, BP311-B, BP311-C, BP311-D) (Jun 18, 2026)

FDA data resources