FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
Brainomix 360 e-CTA
K Number: K242123
·
Decision Jan 6, 2025
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
13
Review Days
171
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Basic Information
- Device Name
- Brainomix 360 e-CTA
- K Number
- K242123
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Brainomix Limited
- Date Received
- July 19, 2024
- Decision Date
- January 6, 2025
- Product Code
- LLZ
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LLZ | System, Image Processing, Radiological | FDA class 2 | Radiology |
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Other Clearances by Brainomix Limited
| K Number | Device Name | ||
|---|---|---|---|
| K260406 | Brainomix 360 Hyperdensity | Jun 12, 2026 | Substantially Equivalent |
| K251983 | Brainomix 360 Triage Stroke | Aug 26, 2025 | Substantially Equivalent |
| K242411 | Brainomix 360 e-Lung | Feb 19, 2025 | Substantially Equivalent |
| K243294 | Brainomix 360 e-ASPECTS | Feb 14, 2025 | Substantially Equivalent |
| K233875 | Brainomix 360 e-Lung | May 13, 2024 | Substantially Equivalent |
| K232496 | Brainomix 360 Triage Stroke | Nov 21, 2023 | Substantially Equivalent |
| K231837 | Brainomix 360 Triage LVO | Sep 28, 2023 | Substantially Equivalent |
| K231656 | Brainomix 360 e-MRI | Aug 30, 2023 | Substantially Equivalent |
| K231195 | Brainomix 360 Triage ICH | Jul 27, 2023 | Substantially Equivalent |
| K223555 | Brainomix 360 e-CTP | Jun 1, 2023 | Substantially Equivalent |