# Alexon, Inc.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 10 (1991–1994): 10 510(k) clearances
- Product codes: MHI (8), MHJ (1), LLH (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
- K934493: Prospect Microplate Assay (Sep 20, 1994)
- K942098: Prospect Giardia (Sep 9, 1994)
- K931147: Prospect (TM) Giardia Rapid Assay, Modification (May 13, 1993)
- K930451: Prospec T Giardia Microtiter Assay (Apr 21, 1993)
- K922675: Prospect Giardia Controls (Sep 11, 1992)
- K922010: Prospect (TM) Giardia Microtiter Assay/Modification (Jun 19, 1992)
- K920817: Modification Prospect Giardia Rapid Assay (Apr 22, 1992)
- K912242: Prospect (TM/Cryptosporidium (Mar 23, 1992)

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