Iomed, Inc.
Iomed, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2007.
Top product codes for Iomed, Inc.
Recent clearances by Iomed, Inc.
- K063465 — CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE
- K060236 — MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODE
- K033192 — RH-950
- K031115 — RH-900
- K001522 — TRANSQ3
- K001410 — PHORESOR MODEL PM2000
- K982668 — PHORESOR II,MODEL PM900
- K974855 — PHORESOR II, MODEL PM900
- K954126 — TRANSQ ELECTRODE PHORESOR II
- K932620 — RH-806/GS MODEL TRANSQ(R)2
- K932621 — RH-801/GS MODEL TRANSQ(R)1
- K934335 — PHORESOR II AUTO, MODEL PM800 MODIFICATION
- K925800 — RH-806, MODEL TRANSQ
- K925806 — RH-801, MODEL TRANSQ
- K914264 — TRANSQ 2
- K914621 — IONTOPHORESIS DEVICE, MODIFICATION
- K896444 — IONTOPHORESIS DEVICE - ELECTRODE RH 800
Data sourced from openFDA. This site is unofficial and independent of the FDA.