HOD — Clamp, Eyelid, Ophthalmic Class I
FDA Device Classification
Classification Details
- Product Code
- HOD
- Device Class
- Class I
- Regulation Number
- 886.4350
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K924774 | r.h. burton | BURTON AUTOMATIC PROJECTOR - MODEL CP-40 | April 14, 1993 |
| K891610 | keeler instruments | HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER | June 5, 1989 |
| K831285 | richard r. anthony, m.d | SURGICAL/LID MARGIN COVER & EYELASH- | June 3, 1983 |