The following data is part of a premarket notification filed by Resound Corp. with the FDA for Resound Personal Hearing System Bt-p W/phs Bt-p.
Device ID | K931942 |
510k Number | K931942 |
Device Name: | RESOUND PERSONAL HEARING SYSTEM BT-P W/PHS BT-P |
Classification | Hearing Aid, Air Conduction |
Applicant | RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
Contact | Jeanette Johnson |
Correspondent | Jeanette Johnson RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-04-19 |
Decision Date | 1993-07-20 |