GDM
- Product code
- GDM
- Device name
- Needle, Aspiration And Injection, Reusable
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 48
Official FDA classification page: GDM
Classification and pathway per current FDA publications. Data from openFDA (CC0).