PDG

Electrosurgical Vessel And/Or Tissue Sealer. With Built-In Generator.

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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: PDG
Classification and pathway per current FDA publications. Data from openFDA (CC0).