OEG

Autoantibodies, Skin (Bullous Pemphigoid 180 And Bullous Pemphigoid 230

Product code: OEG
Device name: Autoantibodies, Skin (Bullous Pemphigoid 180 And Bullous Pemphigoid 230
Device class: Class 2
21 CFR: 21 CFR 866.5660
Medical specialty: Immunology
Marketing pathway: 510(K)
Flag: Third-party review eligible
510(k) clearances (all years, FDA): 3 (all years; only the last 3 years are listed here)

FDA classification definition

The device is intended as an aid in the diagnosis of bullous pemphigoid.

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

Official FDA classification page: OEG

Classification and pathway per current FDA publications. Data from openFDA (CC0).