Company ยท US
Amplifon S.P.A.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 1999. 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 |
|---|---|---|---|
| Sep 20, 1999 | K992370 | AMPLAID A724 AND A728 Amplifon S.P.A. | ETY |
| Jan 29, 1999 | K983915 | AMPLAID A315 AND A319 Amplifon S.P.A. | EWO |
| Jan 12, 1999 | K983712 | AMPLAID A311 SERIES Amplifon S.P.A. | EWO |
| Mar 16, 1998 | K971740 | AMPLAID MK12 Amplifon S.P.A. | GWF |
| Feb 10, 1998 | K974235 | AMPLAID AM50 Amplifon S.P.A. | ETY |
| Feb 6, 1998 | K972959 | AMPLAID MK22 Amplifon S.P.A. | GWF |
| Oct 31, 1997 | K972862 | AMPLAID 171S Amplifon S.P.A. | EWO |
| Aug 5, 1997 | K971747 | AMPLAID 460 Amplifon S.P.A. | EWO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||