LGB — Gonococcal Antibody Tests Class III
FDA product code LGB covers "Gonococcal Antibody Tests", a Class III medical device regulated under 21 CFR 866.3290. Submissions are reviewed by the Microbiology panel.
Classification Details
- Product Code
- LGB
- Device Class
- Class III
- Regulation Number
- 866.3290
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No