Catalogue number OC-ABR, listed by Otodynamics, Ltd., United Kingdom, under Stimulator, Auditory, Evoked Response. 4 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Guangdong (2), Jiangsu (1), Shaanxi (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for Otocheck – ABR Screener | Listed by | Otodynamics, Ltd., United Kingdom |
| FDA product code | GWJ |
| Device type | Stimulator, Auditory, Evoked Response |
| Device class | Class 2 |
| Regulation | 21 CFR 882.1900 |
| Establishment | Manufacturer |
| 510(k) | K143395 |
| Record published | 2016-08-11 |
| Record revised | 2018-07-06 (version 3) |
Specifications
Specifications | MRI safety | MR Unsafe |
| Label carries | manufacturing date, serial number |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.