KLK
- Product code
- KLK
- Device name
- Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia
- Device class
- Class 2
- 21 CFR
- 21 CFR 868.2500
- Medical specialty
- Anesthesiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 47
Official FDA classification page: KLK
Classification and pathway per current FDA publications. Data from openFDA (CC0).