Handheld, portable, Automated Auditory Brainstem Response (AABR) analyser for hearing screening. Includes Otoport Pro instrument, ear probe, system items, and ABR Screener licence
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 Otoport Pro Screener Aabr | 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) | K240430 |
| Record published | 2024-07-17 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| 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.