HOM — Screen, Tangent, Ac-Powered (Campimeter) Class I
FDA product code HOM covers "Screen, Tangent, Ac-Powered (Campimeter)", a Class I medical device regulated under 21 CFR 886.1810. Submissions are reviewed by the Ophthalmic panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- HOM
- Device Class
- Class I
- Regulation Number
- 886.1810
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K860642 | biosan laboratories | PHOTRON VISUAL FIELD ANALYZER | April 15, 1986 |