# King & Spalding

- Location (FDA's records): Washington, DC
- FDA decisions: 7 (1994–1995): 7 510(k) clearances
- Product codes: LZK (2), DXN (2), FWP (1), MIB (1), FZP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Panasonic Corporation (Panasonic): 2 (https://510kreport.com/company/panasonic-panasonic)
- Matsushita Electric Corp. of America: 1 (https://510kreport.com/company/matsushita-electric-of-america)
- Weck Closure Systems: 1 (https://510kreport.com/company/weck-closure-systems)

## Its most-cited devices
- K942422: Panasonic Wrist Blood Pressure Meter (1995), cited by 3
- K941972: Hemo-O-Lok (1994), cited by 1

## Recent decisions
- K942423: Nais Wrist Blood Pressure Meter (Feb 15, 1995)
- K942422: Panasonic Wrist Blood Pressure Meter (Feb 15, 1995)
- K945998: Chin Implant Style I (Feb 7, 1995)
- K944408: Implantech Medical Grade Silicone Sheeting (Nov 9, 1994)
- K942421: Implantech Lateral Mandibular Bar Implant (Aug 8, 1994)
- K942420: Implantech Midface-Submalar LE Fort Implant (Aug 8, 1994)
- K941972: Hemo-O-Lok (Jun 29, 1994)

Source page: https://510kreport.com/company/king-spalding