# E-Med Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1979–1998): 3 510(k) clearances
- Product codes: KMK (1), KRA (1), NAD (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 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
- Scimed Life Systems, Inc.: 1 (https://510kreport.com/company/scimed-life-systems)
- Cardio-Dynamics, Inc.: 1 (https://510kreport.com/company/cardio-dynamics)

## Firms that cite its devices most
- Kerberos Proximal Solutions, Inc.: 1 (https://510kreport.com/company/kerberos-proximal-solutions)

## Its most-cited devices
- K971619: Microfuse Membrane Infusion Catheter (1998), cited by 1

## Recent decisions
- K971619: Microfuse Membrane Infusion Catheter (Feb 27, 1998)
- K843200: Site Strip (Mar 12, 1985)
- K792049: I.V. Strip (Nov 20, 1979)

Source page: https://510kreport.com/company/e-med