# Cambridge Biotech Corp.

- Location (FDA's records): Rockville, MD
- FDA decisions: 3 (1991–1998): 3 510(k) clearances
- Product codes: LSR (2), LLH (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
- Meridian Diagnostics, Inc.: 1 (https://510kreport.com/company/meridian-diagnostics)

## Its most-cited devices
- K911958: Cytoclone a & B Eia (1991), cited by 1

## Recent decisions
- K971169: Cambridge Biotech Human Lyme Igg Western Blot (90111) (Feb 17, 1998)
- K971170: Cambridge Biotech Human Lyme Igm Western Blot (90112) (Feb 17, 1998)
- K911958: Cytoclone a & B Eia (Jul 30, 1991)

Source page: https://510kreport.com/company/cambridge-biotech