510(k) K260529
K260529 is an FDA 510(k) premarket notification submitted by Xiamen High Top Electronic Technology Co., Ltd. for the device "Air Compression Massager (HY-1165)". The FDA issued a decision of Substantially Equivalent on Jul 27, 2026. The device falls under product code IRP (Massager, Powered Inflatable Tube), a Class II device regulated under 21 CFR 890.5650. Xiamen High Top Electronic Technology Co., Ltd. has 1 other 510(k) clearance on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 27, 2026
- Date Received
- Feb 17, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Massager, Powered Inflatable Tube
- Device Class
- Class II
- Regulation Number
- 890.5650
- Review Panel
- PM
- Submission Type
- 510(k)