MULTIX Impact E
by Siemens Medical Solutions USA, Inc.
510(k) K220919
MULTIX Impact E is a Class II device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K220919 on 17 May 2022, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK220919 | Date17 May 2022 | StatusActive |
Official records
- FDA 510(k) database K220919
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KPR
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1680
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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