Company ยท US
Vicon Instrument Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1981. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 15, 1981 | K811751 | FINETONE MODEL VI HEARING AID Vicon Instrument Co. | ESD |
| Aug 3, 1979 | K790878 | SCREENING AUDIOMETER, HIGH FREQUENCY Vicon Instrument Co. | EWO |
| Feb 16, 1979 | K790064 | TINNITUS DEVICES Vicon Instrument Co. | ETS |
| Jan 3, 1978 | K771769 | TINNITUS MASKERS, MODELS S564&S574 Vicon Instrument Co. | KLW |
| Oct 4, 1977 | K771762 | MODULAR HEARING DEVICE, MODEL S291 Vicon Instrument Co. | ESD |
| Jun 28, 1977 | K770938 | TINNITUS AID, MODEL S244 Vicon Instrument Co. | KLW |
| Dec 16, 1976 | K761216 | HEARING AIDS (MODEL E-552 S-712) Vicon Instrument Co. | ESD |
| Jul 21, 1976 | K760215 | HEARING AID, S-522 FM Vicon Instrument Co. | ESD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||