PDG
- Product code
- PDG
- Device name
- Electrosurgical Vessel And/Or Tissue Sealer. With Built-In Generator.
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.4400
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 1
FDA classification definition
Intended for any procedure where vessel ligation (cutting and sealing), soft tissue grasping and dissection are performed.
Official FDA classification page: PDG
Classification and pathway per current FDA publications. Data from openFDA (CC0).