HOJ — Screen, Tangent, Target Class I
FDA Device Classification
Classification Details
- Product Code
- HOJ
- 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 |
|---|
| K873919 | richmond products | TANGENT SCREEN | October 28, 1987 |
| K844657 | pro design intl | SPECTABLE FRAME MAGNIFYING BRILLETTE | December 11, 1984 |
| K821081 | medical equipment designs | CHART PROJECTOR | June 14, 1982 |