lock release 01
lock release 01 (118510) is a Class II device made by NORAS MRI products GmbH, cleared under FDA 510(k) K071179 on 13 Jun 2007 and listed in FDA GUDID since 13 Jul 2018 (UDI-DI 04251269204883), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04251269204883 | Date13 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK071179 | Date13 Jun 2007 | StatusActive |
Official records
- AccessGUDID record 04251269204883
- FDA 510(k) database K071179
Across registries
- FDA 510(k) K071179 decided 13 Jun 2007 Active
- FDA GUDID UDI-DI 04251269204883 listed 13 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K071179
- Listed FDA GUDID 04251269204883
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- lock release
- Generic name
- MRI system coil, radio-frequency
- Model / Ref / Catalog
- 01, 118510
- Primary DI / UDI-DI
- 04251269204883
- 510(k) Number
- FDA product code
- MOS
- GMDN term
- MRI system coil, radio-frequency
- Device class
- Class II
- Regulation number
- 892.1000
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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