# Glaxo, Inc.

- Location (FDA's records): Research Triangle, NC
- FDA decisions: 4 (1984–1995): 4 510(k) clearances
- Product codes: KCD (1), CAF (1), KZH (1), FMI (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
- K954041: G.R.E.E.N. Disposal Container (Note: G.R.E.E.N. IS an Acronym for Glaxo Retrieval Effort for Expended Needles) (Oct 16, 1995)
- K922187: Compact Spacer (Nov 20, 1992)
- K901803: Syringe Needle Introducer (Nov 20, 1990)
- K844169: Volumatic (Nov 9, 1984)

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