FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
XBeam (v2)
K Number: K240671
·
Decision Dec 4, 2024
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
3
Review Days
268
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Basic Information
- Device Name
- XBeam (v2)
- K Number
- K240671
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Xstrahl, Ltd.
- Date Received
- March 11, 2024
- Decision Date
- December 4, 2024
- Product Code
- MUJ
- 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 |
|---|---|---|---|
| MUJ | System, Planning, Radiation Therapy Treatment | FDA class 2 | Radiology |
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