MHI
- Product code
- MHI
- Device name
- Giardia Spp.
- Device class
- Class 2
- 21 CFR
- 21 CFR 866.3220
- Medical specialty
- Microbiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 27 (all years; only the last 3 years are listed here)
Official FDA classification page: MHI
Classification and pathway per current FDA publications. Data from openFDA (CC0).