# K874849: Prospect/Giardia

- Pathway: 510(k) (Traditional)
- Applicant: Alexon Biomedical, Inc.
- Decided: Jan 5, 1988 after 41 days
- Product code: KHW (Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.)
- Device class: 2
- Regulation: 21 CFR 866.3220
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

Source page: https://510kreport.com/device/K874849
Methodology: https://510kreport.com/methodology