HMH — Rack, Skiascopic Class I
FDA Device Classification
Classification Details
- Product Code
- HMH
- Device Class
- Class I
- Regulation Number
- 886.1750
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K844364 | luneau laboratories | SKIASCOPIC RACKS | January 2, 1985 |
| K843195 | visitec | VISITEC FLIERINGA-LEGRAND FIXATION RING | October 5, 1984 |