HJS — Test, Spectacle Dissociation, Ac-Powered (Lancaster) Class I
FDA product code HJS covers "Test, Spectacle Dissociation, Ac-Powered (Lancaster)", a Class I medical device regulated under 21 CFR 886.1910. Submissions are reviewed by the Ophthalmic panel.
Classification Details
- Product Code
- HJS
- Device Class
- Class I
- Regulation Number
- 886.1910
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No