MIM-Thin Client (mobile)
510(k) K151913
MIM-Thin Client (mobile) is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Mim Software Inc., cleared under FDA 510(k) K151913 on 25 Apr 2016, 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 | NumberK151913 | Date25 Apr 2016 | StatusActive |
Official records
- FDA 510(k) database K151913
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- FDA applicant
- Mim Software, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K151913
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 | |||
|---|---|---|---|---|
| MIM 6.7 | 6.7 | 00865936000230 | — | No longer on the market |
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