FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GentleBeam (GB1000)
K Number: K250692
·
Decision Dec 3, 2025
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
52
Applicant Total
1
Review Days
271
Basic Information
- Device Name
- GentleBeam (GB1000)
- K Number
- K250692
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.5900
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Voxel Ray Solutions, LLC
- Date Received
- March 7, 2025
- Decision Date
- December 3, 2025
- Product Code
- JAD
- 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 |
|---|---|---|---|
| JAD | System, Therapeutic, X-Ray | FDA class 2 | Radiology |
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