Duet Drf
by CMT Medical Technologies, Ltd.
510(k) K103038
Duet Drf is a Class II device made by CMT Medical Technologies, Ltd., cleared under FDA 510(k) K103038 on 29 Mar 2011, 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 | NumberK103038 | Date29 Mar 2011 | StatusActive |
Official records
- FDA 510(k) database K103038
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAA
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1650
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K103038
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 | |||
|---|---|---|---|---|
| Duet DRF 63111976 | 63640509 / 63111976 | 07290012104701 | — | On the market |
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