RF-Relief
510(k) K181095
RF-Relief is a Class II device made by El Global Trade Ltd, cleared under FDA 510(k) K181095 on 24 Jul 2018, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK181095 | Date24 Jul 2018 | StatusActive |
Official records
- FDA 510(k) database K181095
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- PBX
- FDA applicant
- El Global Trade, Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 878.4400
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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