Device Classification Name |
Hearing Aid, Air-Conduction, Prescription
|
510(k) Number |
K963607 |
Device Name |
HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANAL |
Applicant |
MIDWEST CITY HEARING AID CENTER |
1401 SOUTH MIDWEST BLVD. |
MIDWEST CITY,
OK
73110
|
|
Applicant Contact |
FRANKLIN D CARTER |
Correspondent |
MIDWEST CITY HEARING AID CENTER |
1401 SOUTH MIDWEST BLVD. |
MIDWEST CITY,
OK
73110
|
|
Correspondent Contact |
FRANKLIN D CARTER |
Regulation Number | 874.3300
|
Classification Product Code |
|
Date Received | 09/09/1996 |
Decision Date | 09/20/1996 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Ear Nose & Throat
|
510k Review Panel |
Ear Nose & Throat
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|