# Columbia Bioscience, Inc.

- Location (FDA's records): Columbia, MD
- FDA decisions: 13 (1996–1999): 13 510(k) clearances
- Product codes: LSE (3), JZO (2), MOB (2), LSR (2), JJQ (2), LYR (1), LJY (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Denley Instruments, Inc.: 2 (https://510kreport.com/company/denley-instruments)
- Anthos Labtec Instruments: 2 (https://510kreport.com/company/anthos-labtec-instruments)
- Anthos Labtec, Inc.: 1 (https://510kreport.com/company/anthos-labtec)

## Recent decisions
- K990462: IS H. Pylori Igg Elisa Test System (Sep 3, 1999)
- K991274: Mumps Igg Elisa Test System (Sep 3, 1999)
- K984228: IS Anti-Tpo Igg Elisa Test System (Feb 2, 1999)
- K983606: IS Borrelia Burgdorferi Igm Test System (Dec 16, 1998)
- K983605: IS Borrelia Burgdorferi Igg/Igm Elisa Test System (Dec 16, 1998)
- K983553: Anti-TG Igg Elisa Test System (Dec 7, 1998)
- K982350: EA-D Igm Elisa Test System (Nov 25, 1998)
- K982348: Ebna-1 Igm Elisa Test System (Nov 25, 1998)

Source page: https://510kreport.com/company/columbia-bioscience