Product code HJB
- Device name
- Instrument, Measuring, Corneal Radius
- Medical specialty
- Ophthalmic
- Device class
- 1
- Regulation number
- 886.1450
- Review panel
- OP
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K930444 | MARCO STANDARD KERATOMETERS | Marco Ophthalmic, Inc. | 1993-08-09 |
| K924779 | BURTON KERATOMETER - MODLE 2040 | R.H. Burton Co. | 1993-04-05 |
| K864369 | LTS CORNEAL MICROSCOPE LASER TOMOGRAPHIC SCANNER | Heidelberg Instruments | 1986-12-15 |
| K864037 | KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER | Kera Corp. | 1986-11-13 |
| K852424 | ACUFEX COMPARATIVE SURGICAL KERATOMETER | Acufex Microsurgical, Inc. | 1985-09-11 |
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