MIM – Dose Analysis
510(k) K232514
MIM – Dose Analysis 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) K232514 on 6 May 2024, active as of 25 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 | NumberK232514 | Date6 May 2024 | StatusActive |
Official records
- FDA 510(k) database K232514
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- Withdrawn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
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