The following data is part of a premarket notification filed by Resound Corp. with the FDA for Resound Custom In-the Canal Hearing Aid Model Ca1.
Device ID | K896463 |
510k Number | K896463 |
Device Name: | RESOUND CUSTOM IN-THE CANAL HEARING AID MODEL CA1 |
Classification | Hearing Aid, Air Conduction |
Applicant | RESOUND CORP. 220 SAGINAW DRIVE, SEAPORT CENTRE Redwood City, CA 94063 |
Contact | Vincent Pluvinage |
Correspondent | Vincent Pluvinage 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 | 1989-11-13 |
Decision Date | 1990-02-08 |