iQMR
by Medic Vision - Imaging Solutions, Ltd.
510(k) K173605
iQMR is a Class II device made by Medic Vision - Imaging Solutions, Ltd., cleared under FDA 510(k) K173605 on 8 Mar 2018, 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 | NumberK173605 | Date8 Mar 2018 | StatusActive |
Official records
- FDA 510(k) database K173605
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K173605
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| iQMR 1.2 | 1.2 | 07290016836400 | — | On the market |
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