FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MULTIX Impact E
K Number: K233532
·
Decision Nov 29, 2023
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
15
Review Days
27
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Basic Information
- Device Name
- MULTIX Impact E
- K Number
- K233532
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 892.1680
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Siemens Medical Solutions
- Date Received
- November 2, 2023
- Decision Date
- November 29, 2023
- Product Code
- KPR
- 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 |
|---|---|---|---|
| KPR | System, X-Ray, Stationary | FDA class 2 | Radiology |
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