The following data is part of a premarket notification filed by Widex Hearing Aid Co., Inc. with the FDA for Widex Model Q9, Bte W/quatro Remote Control.
Device ID | K901316 |
510k Number | K901316 |
Device Name: | WIDEX MODEL Q9, BTE W/QUATRO REMOTE CONTROL |
Classification | Hearing Aid, Air Conduction |
Applicant | WIDEX HEARING AID CO., INC. 35-23 24TH ST. Long Island City, NY 11106 |
Contact | Ron Meltsner |
Correspondent | Ron Meltsner WIDEX HEARING AID CO., INC. 35-23 24TH ST. Long Island City, NY 11106 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-21 |
Decision Date | 1990-04-10 |