# La Jolla Technology, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 5 (1983–1987): 5 510(k) clearances
- Product codes: GXY (2), GZJ (2), DPS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K870160: Dynex Disposable Self-Adhering Electrode W/Tens (Apr 1, 1987)
- K864956: Dynex Iii Transcutaneous Electrical Nerve Stimula. (Mar 9, 1987)
- K854204: Dynex Reusable, Self-Adhering Electrode W/Tens (Jan 10, 1986)
- K832888: Ecg Interference Filter TF-03 (Jan 18, 1984)
- K830932: Nynex II (Apr 18, 1983)

Source page: https://510kreport.com/company/la-jolla-technology