RecoveryRx
510(k) K190251
RecoveryRx is a Class II device made by Bioelectronics Corporation, cleared under FDA 510(k) K190251 on 28 Jun 2019, active as of 11 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 | NumberK190251 | Date28 Jun 2019 | StatusActive |
Official records
- FDA 510(k) database K190251
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ILX
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5290
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
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