Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25)
Summary
Huizhou Lvb Maternal and Infant Supplies Co., Ltd. received 510(k) clearance for Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25), a HGX device. Cleared on 2025-08-13.
Details
Source
510(k) Clearance
External ID
K252192
Action Date
2025-08-13
Status
Special
Category
device
Product Code
HGX
Product Description
Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25). Product code: HGX.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Huizhou Lvb Maternal and Infant Supplies Co., Ltd. has received 3 total clearances in our database.
Huizhou Lvb Maternal and Infant Supplies Co., Ltd. has 3 FDA actions in our database, including 3 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Huizhou Lvb Maternal and Infant Supplies Co., Ltd. have FDA actions?
Huizhou Lvb Maternal and Infant Supplies Co., Ltd. has 3 FDA actions in our database, including 0 recalls and 3 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K252192" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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