# Medicotest A/S

- Location (FDA's records): Washington, DC
- FDA decisions: 7 (1997–2002): 7 510(k) clearances
- Product codes: IKT (3), DRX (2), MKJ (1), GXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (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 that cite its devices most
- Spes Medica Srl: 2 (https://510kreport.com/company/spes-medica)
- Ambu A/S: 2 (https://510kreport.com/company/ambu-a-s)
- Technomed Europe: 1 (https://510kreport.com/company/technomed-europe)
- Rochester Electro Medical, Inc.: 1 (https://510kreport.com/company/rochester-electro-medical)
- Ambu, Inc.: 1 (https://510kreport.com/company/ambu)
- Specialized Laboratory Equipment, Ltd.: 1 (https://510kreport.com/company/specialized-laboratory-equipment)

## Its most-cited devices
- K973529: Neuroline, Disposable Concentric Needle Electrodes (1997), cited by 5
- K001869: Diagnostic Electromyography Needle Electrode, Disposable Hypodermic Needle (2000), cited by 2
- K983689: Blue Sensor Supatab,Disposable Ecg Electrodes (1999), cited by 1

## Recent decisions
- K020382: Blue Sensor, Disposable Ecg Electrodes for Anaesthesia (Jun 28, 2002)
- K020907: Neuroline, Subdermal Needle Electrodes (Jun 14, 2002)
- K002079: Multi-Function Defibrillation Electrode (Feb 22, 2001)
- K001869: Diagnostic Electromyography Needle Electrode, Disposable Hypodermic Needle (Sep 18, 2000)
- K983689: Blue Sensor Supatab,Disposable Ecg Electrodes (Jan 15, 1999)
- K973529: Neuroline, Disposable Concentric Needle Electrodes (Nov 20, 1997)
- K965194: Medicom, Tens Electrodes (Mar 6, 1997)

Source page: https://510kreport.com/company/medicotest-a-s