Device Classification Name |
audiometer
|
510(k) Number |
K790878 |
Device Name |
SCREENING AUDIOMETER, HIGH FREQUENCY |
Applicant |
VICON INSTRUMENT CO. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
VICON INSTRUMENT CO. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 874.1050
|
Classification Product Code |
|
Date Received | 05/07/1979 |
Decision Date | 08/03/1979 |
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
|
|
|