MMS — Lubricant, Vaginal, Patient Class I
FDA product code MMS covers "Lubricant, Vaginal, Patient", a Class I medical device regulated under 21 CFR 880.6375. Submissions are reviewed by the General Hospital panel.
Classification Details
- Product Code
- MMS
- Device Class
- Class I
- Regulation Number
- 880.6375
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- No