Vicon Instrument Co.
FDA 510(k) & PMA Approved Devices — 8 products
Advertisement
Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K811751 | FINETONE MODEL VI HEARING AID | ESD | 1981-07-15 | View |
| 510(k) | K790878 | SCREENING AUDIOMETER, HIGH FREQUENCY | EWO | 1979-08-03 | View |
| 510(k) | K790064 | TINNITUS DEVICES | ETS | 1979-02-16 | View |
| 510(k) | K771769 | TINNITUS MASKERS, MODELS S564&S574 | KLW | 1978-01-03 | View |
| 510(k) | K771762 | MODULAR HEARING DEVICE, MODEL S291 | ESD | 1977-10-04 | View |
| 510(k) | K770938 | TINNITUS AID, MODEL S244 | KLW | 1977-06-28 | View |
| 510(k) | K761216 | HEARING AIDS (MODEL E-552 S-712) | ESD | 1976-12-16 | View |
| 510(k) | K760215 | HEARING AID, S-522 FM | ESD | 1976-07-21 | View |
No matching devices.
Advertisement