Somatom Flash Ds
by Siemens Medical Solutions USA, Inc.
510(k) K082220
Somatom Flash Ds is a Class II device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K082220 on 10 Oct 2008, 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 | NumberK082220 | Date10 Oct 2008 | StatusActive |
Official records
- FDA 510(k) database K082220
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAK
- Device class
- Class II
- Regulation
- 21 CFR Part 892.1750
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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