MIM-Ablation
510(k) K220256
MIM-Ablation is a medical device (FDA Class II; FDA product code QTZ) made by Mim Software Inc., cleared under FDA 510(k) K220256 on 7 Oct 2022, active as of 11 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 | NumberK220256 | Date7 Oct 2022 | StatusActive |
Official records
- FDA 510(k) database K220256
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- QTZ
- FDA applicant
- Mim Software, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code QTZ (Radiological Image Processing Software For Ablation Therapy Planning And Evaluation).