BASEN Wearable Breast Pump (Model: YM-801, YM-803, YM-805, YM-806, YM-808)

FDA 510(k) K231969 · Dongguanshi Yiyingmei Technology Co., Ltd.

Substantially Equivalent

510(k) numberK231969

Submission

Device name
BASEN Wearable Breast Pump (Model: YM-801, YM-803, YM-805, YM-806, YM-808)
Applicant
Dongguanshi Yiyingmei Technology Co., Ltd.
Donguang, CN
Received
July 3, 2023
Decision date
August 30, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HGX – Pump, Breast, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 884.5160
Specialty
Obstetrics/Gynecology

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Questions and answers

When was BASEN Wearable Breast Pump (Model: YM-801, YM-803, YM-805, YM-806, YM-808) cleared by the FDA?

BASEN Wearable Breast Pump (Model: YM-801, YM-803, YM-805, YM-806, YM-808) (K231969) received a 510(k) decision of Substantially Equivalent on August 30, 2024, 424 days after the submission was received.

What is the product code of K231969?

The FDA product code is HGX – Pump, Breast, Powered, a Class II (moderate risk) device regulated under 21 CFR 884.5160.