510(k) K210967
K210967 is an FDA 510(k) premarket notification submitted by Xiamen Weiyou Intelligent Technology Co., Ltd. for the device "Air Pressure Therapy System: VU-IPC06". The FDA issued a decision of Substantially Equivalent on May 11, 2021. The device falls under product code IRP (Massager, Powered Inflatable Tube), a Class II device regulated under 21 CFR 890.5650. Xiamen Weiyou Intelligent Technology Co., Ltd. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 11, 2021
- Date Received
- March 31, 2021
- 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