← FDA Medical Device Classifications
Autoantibodies, Skin (Bullous Pemphigoid 180 And Bullous Pemphigoid 230
OEG · Class II — Moderate Risk (510(k) clearance required) · Immunology · 21 CFR 866.5660
Classification
- FDA Product Code
OEG- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 866.5660
- Review panel
- IM
- Medical specialty
- Immunology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- Y
Definition
The device is intended as an aid in the diagnosis of bullous pemphigoid.
Market data
- Cleared 510(k) submissions
- 3
- Registered establishments
- 4
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown