HJB — Instrument, Measuring, Corneal Radius Class I
FDA Device Classification
Classification Details
- Product Code
- HJB
- Device Class
- Class I
- Regulation Number
- 886.1450
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K930444 | marco ophthalmic | MARCO STANDARD KERATOMETERS | August 9, 1993 |
| K924779 | r.h. burton | BURTON KERATOMETER - MODLE 2040 | April 5, 1993 |
| K864369 | heidelberg instruments | LTS CORNEAL MICROSCOPE LASER TOMOGRAPHIC SCANNER | December 15, 1986 |
| K864037 | kera | KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER | November 13, 1986 |
| K852424 | acufex microsurgical | ACUFEX COMPARATIVE SURGICAL KERATOMETER | September 11, 1985 |