# Stoelting Co.

- Location (FDA's records): Wood Dale, IL
- FDA decisions: 4 (1995–2001): 4 510(k) clearances
- Product codes: HCC (4)
- Predicates its devices cite: 0 (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 that cite its devices most
- Brainmaster: 1 (https://510kreport.com/company/brainmaster)

## Its most-cited devices
- K965006: AT 62 Eeg (a.K.a the a;Pha-Theta Trainer) (1997), cited by 1

## Recent decisions
- K012011: Modification to A620 Eeg (Oct 10, 2001)
- K965006: AT 62 Eeg (a.K.a the a;Pha-Theta Trainer) (Feb 5, 1997)
- K952797: AT53 Dual Channel Emg (Apr 17, 1996)
- K944615: A620 EEG (Sep 18, 1995)

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