GPD — Antigen, Indirect Fluorescent Antibody Test, Echinococcus Granulosus Class I
FDA product code GPD covers "Antigen, Indirect Fluorescent Antibody Test, Echinococcus Granulosus", a Class I medical device regulated under 21 CFR 866.3200. Submissions are reviewed by the Microbiology panel.
Classification Details
- Product Code
- GPD
- Device Class
- Class I
- Regulation Number
- 866.3200
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No