Identifiers
- 510(k) Number
- K251883 FDA 510(k)
- FDA Product Code
- LLZ FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.2050 FDA 510(k)
- Regulation Number
- 892.2050 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
MIM Software, Inc. has submitted a complaint to the FDA regarding the LesionID Pro device for its alleged failure to accurately diagnose and treat brain tumors.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K251883 | Class II | Active |
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Manufacturer
- Manufacturer
- Mim Software Inc.
- FDA Applicant
- Mim Software, Inc.
Sources (1)
- FDA 510(k) K251883 24 fields · synced Jul 15, 2026