# Medicotest, Inc.

- Location (FDA's records): St. Louis, MO
- FDA decisions: 14 (1982–1999): 14 510(k) clearances
- Product codes: GXY (5), DRX (5), GXZ (2), KGX (1), GYB (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (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
- Ambu A/S: 2 (https://510kreport.com/company/ambu-a-s)
- Technomed Europe: 1 (https://510kreport.com/company/technomed-europe)
- Dymedix, Inc.: 1 (https://510kreport.com/company/dymedix)
- Spes Medica Srl: 1 (https://510kreport.com/company/spes-medica)
- Specialized Laboratory Equipment, Ltd.: 1 (https://510kreport.com/company/specialized-laboratory-equipment)

## Its most-cited devices
- K931430: Cutaneous Electrode (1993), cited by 2
- K983597: Neuroline, Disposable Monopolar Needle Electrodes (1999), cited by 1
- K921579: BR-50-J Disposable Ecg Electrode (1992), cited by 1
- K902407: NF-50-E Disposable Ecg Electrode (1990), cited by 1
- K901280: Disposible Eeg Needle Electrodes (1990), cited by 1

## Recent decisions
- K983597: Neuroline, Disposable Monopolar Needle Electrodes (Jan 11, 1999)
- K970639: Neuroline, Disposable Reference and Recording Electrodes Type NO: 72000-S, 72010-K (May 15, 1997)
- K961643: Medicotest Ecg Electrodes (Dec 9, 1996)
- K952176: Disposable Neurology Electrodes Neuroline 7 30 01-K (Sep 25, 1995)
- K941568: K-10-VS, DA-05-VS, Recording Electrodes (Nov 4, 1994)
- K931430: Cutaneous Electrode (Dec 21, 1993)
- K931426: NF-11-E Disposable Reference/Recording Electrode (Dec 21, 1993)
- K926264: Medicotest Skin Fix (Apr 20, 1993)

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