MR5 Activ Pro
510(k) K254024
MR5 Activ Pro is a Class II device made by Multi Radiance Medical, cleared under FDA 510(k) K254024 on 19 May 2026, active as of 12 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 | NumberK254024 | Date19 May 2026 | StatusActive |
Official records
- FDA 510(k) database K254024
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- NHN
- FDA applicant
- Multi Radiance Medical, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5500
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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