The following data is part of a premarket notification filed by Resound Corp. with the FDA for Personal Hearing System.
| Device ID | K944041 |
| 510k Number | K944041 |
| Device Name: | PERSONAL HEARING SYSTEM |
| Classification | I.v. Start Kit |
| Applicant | RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
| Contact | Jeannette S Johnson |
| Correspondent | Jeannette S Johnson RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
| Product Code | LRS |
| CFR Regulation Number | 880.5200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-18 |
| Decision Date | 1994-12-27 |