510(k) K191862
K191862 is an FDA 510(k) premarket notification submitted by Guangzhou Longest Science & Technology Co., Ltd. for the device "Compression Therapy Device Model LGT-2200SP". The FDA issued a decision of Substantially Equivalent on Oct 29, 2019. The device falls under product code IRP (Massager, Powered Inflatable Tube), a Class II device regulated under 21 CFR 890.5650. Guangzhou Longest Science & Technology Co., Ltd. has 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 29, 2019
- Date Received
- Jul 11, 2019
- 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)