KZX
- Product code
- KZX
- Device name
- Kit, Disc, Agar Gel Diffusion, Determine Serum Levels Of Tobramycin
- Device class
- Class 2
- 21 CFR
- 21 CFR 862.3900
- Medical specialty
- Clinical Toxicology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
Official FDA classification page: KZX
Classification and pathway per current FDA publications. Data from openFDA (CC0).