Iomed, Inc.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 17
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K063465 | CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE | February 28, 2007 |
| K060236 | MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE | March 31, 2006 |
| K033192 | RH-950 | December 22, 2003 |
| K031115 | RH-900 | July 10, 2003 |
| K001522 | TRANSQ3 | October 18, 2000 |
| K001410 | PHORESOR MODEL PM2000 | August 1, 2000 |
| K982668 | PHORESOR II,MODEL PM900 | March 2, 1999 |
| K974855 | PHORESOR II, MODEL PM900 | March 27, 1998 |
| K954126 | TRANSQ ELECTRODE PHORESOR II | January 19, 1996 |
| K932621 | RH-801/GS MODEL TRANSQ(R)1 | July 26, 1994 |
| K932620 | RH-806/GS MODEL TRANSQ(R)2 | July 26, 1994 |
| K934335 | PHORESOR II AUTO, MODEL PM800 MODIFICATION | July 26, 1994 |
| K925806 | RH-801, MODEL TRANSQ | July 14, 1994 |
| K925800 | RH-806, MODEL TRANSQ | July 14, 1994 |
| K914264 | TRANSQ 2 | December 20, 1991 |
| K914621 | IONTOPHORESIS DEVICE, MODIFICATION | December 20, 1991 |
| K896444 | IONTOPHORESIS DEVICE - ELECTRODE RH 800 | May 10, 1990 |