The following data is part of a premarket notification filed by Vicon Instrument Co. with the FDA for Screening Audiometer, High Frequency.
| Device ID | K790878 |
| 510k Number | K790878 |
| Device Name: | SCREENING AUDIOMETER, HIGH FREQUENCY |
| Classification | Audiometer |
| Applicant | VICON INSTRUMENT CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EWO |
| CFR Regulation Number | 874.1050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-05-07 |
| Decision Date | 1979-08-03 |