# Medelec, Ltd.

- Location (FDA's records): Old Woking, Surrey, DE
- FDA decisions: 8 (1992–1997): 8 510(k) clearances
- Product codes: GWQ (2), GWF (2), OLT (2), BSZ (1), GWJ (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Carefusion 209, Inc.: 2 (https://510kreport.com/company/carefusion-209)
- Kvikna Ehf: 2 (https://510kreport.com/company/kvikna)
- Viasys Neuro Care: 1 (https://510kreport.com/company/viasys-neuro-care)
- Sacs Medical AB: 1 (https://510kreport.com/company/sacs-medical)

## Its most-cited devices
- K964280: DG Nervus (1997), cited by 4
- K965065: Teca.  Millennium (1997), cited by 2

## Recent decisions
- K965065: Teca.  Millennium (Jun 20, 1997)
- K964280: DG Nervus (Jan 27, 1997)
- K954157: DG Portable System (Jan 17, 1996)
- K953799: DG Examiner Plus (Nov 8, 1995)
- K953732: Teca Premiere (Oct 19, 1995)
- K934670: DG 3P System (May 25, 1994)
- K934669: ARC (Apr 26, 1994)
- K923303: Sapphire Premiere (Nov 24, 1992)

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