510(k) K260239
K260239 is an FDA 510(k) premarket notification submitted by Jiangxi AOV Maternity & Baby Products Co., Ltd. for the device "Wearable Breast Pump (AOV6853, AOV6860, AOV6861, AOV6862)". The FDA issued a decision of Substantially Equivalent on April 22, 2026. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Jiangxi AOV Maternity & Baby Products Co., Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 22, 2026
- Date Received
- January 26, 2026
- 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