Company ยท US
Finetone Hearing Instruments
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1998. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Feb 20, 1998 | K974219 | FACEPLATE ASSEMBLY Finetone Hearing Instruments | LRB |
| Feb 2, 1996 | K955692 | FINETONE FSC, Finetone Hearing Instruments | ESD |
| Dec 21, 1994 | K945780 | FINETONE DISCEET CANAL Finetone Hearing Instruments | ESD |
| Jun 29, 1994 | K940164 | SUPER-SIL Finetone Hearing Instruments | ESD |
| Jun 30, 1983 | K830960 | CUSTOM IN-THE-EAR HEARING AID Finetone Hearing Instruments | ESD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||