NJG — Flasher, Afterimage, Ophthalmic Class II
FDA product code NJG covers "Flasher, Afterimage, Ophthalmic", a Class II medical device regulated under 21 CFR 886.1300. Submissions are reviewed by the Ophthalmic panel.
Classification Details
- Product Code
- NJG
- Device Class
- Class II
- Regulation Number
- 886.1300
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No