# Kay Elemetrics Corp.

- Location (FDA's records): Lincoln Park, NJ
- FDA decisions: 5 (1992–1999): 5 510(k) clearances
- Product codes: EQL (2), KLA (1), LLZ (1), KLX (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
- MethodSense, Inc.: 1 (https://510kreport.com/company/methodsense)

## Its most-cited devices
- K991738: Digital Video Recording System (1999), cited by 1

## Recent decisions
- K991738: Digital Video Recording System (Aug 13, 1999)
- K990240: Electroglottograph (Mar 11, 1999)
- K954798: 7100 Swallowing Workstation (Jun 4, 1996)
- K921184: RLS 9100 Rhino-Laryngeal Stroboscope (May 28, 1992)
- K921285: 9105 Rigid Telescopic Endoscope (May 28, 1992)

Source page: https://510kreport.com/company/kay-elemetrics