MZM — Fibrin Sealant Preparation Device Class II
FDA product code MZM covers "Fibrin Sealant Preparation Device", a Class II medical device regulated under 21 CFR 880.5860. Submissions are reviewed by the General Hospital panel.
Classification Details
- Product Code
- MZM
- Device Class
- Class II
- Regulation Number
- 880.5860
- Submission Type
- Review Panel
- HE
- Medical Specialty
- General Hospital
- Implant
- No