# Lkc Technologies, Inc.

- Location (FDA's records): Gaithersburg, MD
- FDA decisions: 8 (1976–2015): 8 510(k) clearances
- Product codes: HLX (1), HPT (1), HIT (1), DRG (1), GWE (1), HLZ (1), GWF (1), HIW (1)
- 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
- Electro-Diagnostic Imaging, Inc.: 1 (https://510kreport.com/company/electro-diagnostic-imaging)

## Its most-cited devices
- K760199: Electroretinograph (1976), cited by 1

## Recent decisions
- K142567: RETeval Visual Electrodiagnostic Device (May 19, 2015)
- K914163: Scoptopic Sensitivity Test-1[SST-1] (Oct 25, 1991)
- K913962: Anomaloscope Quadrant Test-6 (Oct 23, 1991)
- K875026: Anomaloscope Plate Test - 5 [Apt-5] (Feb 5, 1988)
- K874336: Pattern Discrimination Perimeter (Jan 12, 1988)
- K820414: Universal Testing & Analysis Systems (Mar 4, 1982)
- K790109: Telemetry, Biomedical (Mar 16, 1979)
- K760199: Electroretinograph (Aug 4, 1976)

Source page: https://510kreport.com/company/lkc-technologies