K220034
- 510(k) number
- K220034
- Device name
- NEUROShield
- Applicant
- In-Med Prognostics L3c CA · US
- Product code
- LLZ — System, Image Processing, Radiological
- Decision date
- 2023-09-14
- Date received
- 2022-01-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
Official FDA record: K220034
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.