KXG
- Product code
- KXG
- Device name
- Applicator, Absorbent Tipped, Sterile
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.6025
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: KXG
Classification and pathway per current FDA publications. Data from openFDA (CC0).