Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Autoantibodies, Skin (Bullous Pemphigoid 180 And Bullous Pemphigoid 230

FDA product code OEG · 3 cleared devices

Class 2 Immunology
Regulation
21 CFR 866.5660
Review panel
IM
Implant
No
Life sustaining
No
Third party review
Yes
GMP exempt
No
Clearance span
2008-08-25 – 2020-09-17

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

↑