KMF
- Product code
- KMF
- Device name
- Bandage, Liquid
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.5090
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 222
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K241916 | 2024-09-27 | Optmed, Inc. | TearRepair Liquid Skin Protectant |
Official FDA classification page: KMF
Classification and pathway per current FDA publications. Data from openFDA (CC0).