Visual Stimulation Box M014700
by Intelligent Hearing Systems Corp.
Visual Stimulation Box M014700 is a Class II device made by Intelligent Hearing Systems Corp., cleared under FDA 510(k) K070608 on 18 Jul 2007 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00817020020457), 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 | GUDID listing | Number00817020020457 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK070608 | Date18 Jul 2007 | StatusActive |
Official records
- AccessGUDID record 00817020020457
- FDA 510(k) database K070608
Across registries
- FDA 510(k) K070608 decided 18 Jul 2007 Active
- FDA GUDID UDI-DI 00817020020457 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K070608
- Listed FDA GUDID 00817020020457
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Visual Stimulation Box
- Generic name
- Visual stimulator
- Model / reference
- M014700
- Primary DI / UDI-DI
- 00817020020457
- 510(k) Number
- FDA product code
- GWE
- GMDN term
- Visual stimulator
- Device class
- Class II
- Regulation number
- 882.1890
- GUDID distribution status
- In Commercial Distribution
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