# Positron

- Location (FDA's records): Houston, TX
- FDA decisions: 5 (1981–2002): 5 510(k) clearances
- Names in FDA's records: Positron (4); Positron Corp. (1)
- Product codes: KPS (4), EWO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Neusoft Positron Medical Systems Co., Ltd.: 1 (https://510kreport.com/company/neusoft-positron-medical-systems)
- GE Healthcare: 1 (https://510kreport.com/company/ge-healthcare)

## Its most-cited devices
- K022001: Mpower, Model 712 Series (2002), cited by 2

## Recent decisions
- K022001: Mpower, Model 712 Series (Jul 12, 2002)
- K926206: Posicam-HZ & Posicam-HZL (Jul 8, 1993)
- K911275: Posicam System Model 6.5 Posicam-HZ System (May 9, 1991)
- K894998: Modified Posicam System Model 6.5 (Nov 2, 1989)
- K810537: Automatic Screening Audiometer (Mar 11, 1981)

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