Company ยท US
American Imex
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 2004. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 11 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 7, 2004 | K032003 | PREMIER PLUS American Imex | GZJ |
| Sep 22, 1998 | K982221 | PREMIER AP American Imex | GZJ |
| Jun 1, 1993 | K926326 | MICROCARE(TM) American Imex | GZJ |
| Nov 22, 1991 | K912289 | ULTIMA XS, MODIFICATION American Imex | GZJ |
| Nov 6, 1989 | K895295 | ULTIMA XS MICROCURRENT TENS American Imex | GZJ |
| Aug 10, 1989 | K894388 | ZIMMER TENS American Imex | GZJ |
| May 4, 1988 | K881704 | EASY TENS American Imex | GZJ |
| Apr 11, 1988 | K881424 | PREMIER 10S (TENS) American Imex | GZJ |
| Apr 6, 1988 | K880751 | ULTIMA XS (TENS) American Imex | GZJ |
| Feb 20, 1987 | K864735 | A-TENS - MODEL AI-87 American Imex | GZJ |
| May 16, 1986 | K861709 | A TENS (MODEL AI-86) American Imex | GZJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||