FMC
- Product code
- FMC
- Device name
- Patient Examination Glove
- Device class
- Class 1
- 21 CFR
- 21 CFR 880.6250
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 34
Official FDA classification page: FMC
Classification and pathway per current FDA publications. Data from openFDA (CC0).