HIW — Anomaloscope Class I
FDA Device Classification
Classification Details
- Product Code
- HIW
- Device Class
- Class I
- Regulation Number
- 886.1070
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K930575 | bova intl | KAMPPETER ANOMALOSCOPE | February 25, 1994 |
| K913962 | lkc technologies | ANOMALOSCOPE QUADRANT TEST-6 | October 23, 1991 |
| K860174 | chromagraphics | GUNKEL CHROMAGRAPH COLOR VISION TESTER | April 4, 1986 |