# OMG: Antisera, Fluorescent, Human Metapneumovirus

- Device class: 2; regulation: 21 CFR 866.3980; FDA's rule: 510(k) required
- FDA decisions: 4
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2009: 3
- 2010: 1

## Most-cited predicates
- K090073: D3 Dfa Metapneumovirus Identification Kit (2009), cited by 2

Source page: https://510kreport.com/product-code/OMG
Data by year (CSV): https://510kreport.com/product-code/OMG.csv