iMAR
by Siemens Medical Solutions USA, Inc.
510(k) K142584
iMAR is a Class II device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K142584 on 16 Jan 2015, 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 | NumberK142584 | Date16 Jan 2015 | StatusActive |
Official records
- FDA 510(k) database K142584
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- Withdrawn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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