HOK — Screen, Tangent, Projection, Ac-Powered Class I
FDA product code HOK covers "Screen, Tangent, Projection, Ac-Powered", a Class I medical device regulated under 21 CFR 886.1810. Submissions are reviewed by the Ophthalmic panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- HOK
- Device Class
- Class I
- Regulation Number
- 886.1810
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K914896 | clement clarke | FRIEDMANN ANALYSER 3 | January 23, 1992 |