HJJ — Lens, Fresnel, Flexible, Diagnostic Class I
FDA product code HJJ covers "Lens, Fresnel, Flexible, Diagnostic", a Class I medical device regulated under 21 CFR 886.1390. Submissions are reviewed by the Ophthalmic panel.
Classification Details
- Product Code
- HJJ
- Device Class
- Class I
- Regulation Number
- 886.1390
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No