Company ยท US
Iomed, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 2007. Name variants (Inc, Corp, punctuation) are merged.
17510(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 28, 2007 | K063465 | CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE Iomed, Inc. | EGJ |
| Mar 31, 2006 | K060236 | MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE Iomed, Inc. | EGJ |
| Dec 22, 2003 | K033192 | RH-950 Iomed, Inc. | KTB |
| Jul 10, 2003 | K031115 | RH-900 Iomed, Inc. | KTB |
| Oct 18, 2000 | K001522 | TRANSQ3 Iomed, Inc. | KTB |
| Aug 1, 2000 | K001410 | PHORESOR MODEL PM2000 Iomed, Inc. | KTB |
| Mar 2, 1999 | K982668 | PHORESOR II,MODEL PM900 Iomed, Inc. | EGJ |
| Mar 27, 1998 | K974855 | PHORESOR II, MODEL PM900 Iomed, Inc. | KTB |
| Jan 19, 1996 | K954126 | TRANSQ ELECTRODE PHORESOR II Iomed, Inc. | KTB |
| Jul 26, 1994 | K934335 | PHORESOR II AUTO, MODEL PM800 MODIFICATION Iomed, Inc. | EGJ |
| Jul 26, 1994 | K932621 | RH-801/GS MODEL TRANSQ(R)1 Iomed, Inc. | EGJ |
| Jul 26, 1994 | K932620 | RH-806/GS MODEL TRANSQ(R)2 Iomed, Inc. | EGJ |
| Jul 14, 1994 | K925806 | RH-801, MODEL TRANSQ Iomed, Inc. | EGJ |
| Jul 14, 1994 | K925800 | RH-806, MODEL TRANSQ Iomed, Inc. | EGJ |
| Dec 20, 1991 | K914621 | IONTOPHORESIS DEVICE, MODIFICATION Iomed, Inc. | EGJ |
| Dec 20, 1991 | K914264 | TRANSQ 2 Iomed, Inc. | EGJ |
| May 10, 1990 | K896444 | IONTOPHORESIS DEVICE - ELECTRODE RH 800 Iomed, Inc. | EGJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||