OAE 10D Probe M032103G
by Intelligent Hearing Systems Corp.
OAE 10D Probe M032103G is a Class II device made by Intelligent Hearing Systems Corp., cleared under FDA 510(k) K023859 on 8 Jan 2003 (1 earlier submission) and listed in FDA GUDID since 14 May 2018 (UDI-DI 00817020029993), 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 | Number00817020029993 | Date14 May 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK023859 | Date8 Jan 2003 | StatusActive |
Official records
- AccessGUDID record 00817020029993
- FDA 510(k) database K023859
- FDA 510(k) database K964426
Across registries
- FDA 510(k) K023859 decided 8 Jan 2003 Active
- FDA GUDID UDI-DI 00817020029993 listed 14 May 2018 Listed
Timeline
- Cleared FDA 510(k) K964426
- Cleared FDA 510(k) K023859
- Listed FDA GUDID 00817020029993
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- OAE 10D Probe
- Generic name
- Otoacoustic emission system, line-powered
- Model / reference
- M032103G
- Primary DI / UDI-DI
- 00817020029993
- FDA product code
- EWO
- GMDN term
- Otoacoustic emission system, line-powered
- Device class
- Class II
- Regulation number
- 874.1050
- GUDID distribution status
- In Commercial Distribution