Rmf-2000
510(k) K220073
Rmf-2000 is a Class II device made by DRTECH Corporation, cleared under FDA 510(k) K220073 on 26 Jan 2023, 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 | NumberK220073 | Date26 Jan 2023 | StatusActive |
Official records
- FDA 510(k) database K220073
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MUE
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1715
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K220073
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| AIDIA RMF-2000 | RMF-2000 | 08800018423004 | — | On the market |
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