Mrt 50A Joint Coil
510(k) K900727
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK900727 | Date9 Mar 1990 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- LNH
- Device Class
- Class II
- Regulation
- 21 CFR Part 892.1000
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 21 Sep 2026
The Mrt 50A Joint Coil is a Nuclear Magnetic Resonance Imaging device, classified as a System. It is used in the field of Radiology.
The device is supplied with a product code of LNH and has been cleared under the FDA 510K number K900727. It is a Class II device, regulated under regulation number 892.1000.
Other devices from Toshiba America Mri, Inc.
Questions
AI-generated answers, 21 Sep 2026
What is the MRT 50A Joint Coil used for?
The MRT 50A Joint Coil is used in the field of Radiology for Nuclear Magnetic Resonance Imaging.
Is the MRT 50A Joint Coil a single-use or reusable device?
The device data does not specify whether the MRT 50A Joint Coil is single-use or reusable, it is classified as a System.
What is the regulatory classification of the MRT 50A Joint Coil?
The MRT 50A Joint Coil is a Class II device, regulated under regulation number 892.1000.