HRE — Cabinet, Instrument, Ac-Powered, Ophthalmic Class I
FDA product code HRE covers "Cabinet, Instrument, Ac-Powered, Ophthalmic", a Class I medical device regulated under 21 CFR 886.1860. Submissions are reviewed by the Ophthalmic panel.
Classification Details
- Product Code
- HRE
- Device Class
- Class I
- Regulation Number
- 886.1860
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No