# Iomed, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 17 (1990–2007): 17 510(k) clearances
- Product codes: EGJ (11), KTB (6)
- Predicates its devices cite: 11 (9 its own); citations of its devices by later devices: 34 (9 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mattioli Engineering Corp.: 1 (https://510kreport.com/company/mattioli-engineering)
- Empi: 1 (https://510kreport.com/company/empi)

## Firms that cite its devices most
- Empi: 6 (https://510kreport.com/company/empi)
- Selectivemed Components, Inc.: 4 (https://510kreport.com/company/selectivemed-components)
- Medical Adhesiveonline, LLC: 2 (https://510kreport.com/company/medical-adhesiveonline)
- Pepin Mfg., Inc.: 2 (https://510kreport.com/company/pepin-mfg)
- Vyteris, Inc.: 2 (https://510kreport.com/company/vyteris)
- Activatek, Inc.: 2 (https://510kreport.com/company/activatek)
- Naimco, Inc.: 2 (https://510kreport.com/company/naimco)
- North Coast Medical, Inc.: 2 (https://510kreport.com/company/north-coast-medical)

## Its most-cited devices
- K932620: RH-806/GS Model Transq (R)2 (1994), cited by 6
- K932621: RH-801/GS Model Transq (R)1 (1994), cited by 6
- K982668: Phoresor II,Model PM900 (1999), cited by 4
- K974855: Phoresor II, Model PM900 (1998), cited by 4
- K934335: Phoresor II Auto, Model PM800 Modification (1994), cited by 3
- K914621: Iontophoresis Device, Modification (1991), cited by 2

## Recent decisions
- K063465: Champion Iontophoretic Drug Delivery Device (Feb 28, 2007)
- K060236: MW-1000 Iontophoretic Drug Delivery Electrode (Mar 31, 2006)
- K033192: RH-950 (Dec 22, 2003)
- K031115: RH-900 (Jul 10, 2003)
- K001522: TRANSQ3 (Oct 18, 2000)
- K001410: Phoresor Model PM2000 (Aug 1, 2000)
- K982668: Phoresor II,Model PM900 (Mar 2, 1999)
- K974855: Phoresor II, Model PM900 (Mar 27, 1998)

Source page: https://510kreport.com/company/iomed