Product code HOM— Ophthalmic
PHOTRON VISUAL FIELD ANALYZER
- Classification name
- Screen, Tangent, Ac-Powered (Campimeter)
- Device class
- Class 1
- Regulation
- 21 CFR 886.1810
- Advisory panel
- Ophthalmic
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code HOM
FDA has cleared device under product code HOM, all in 1986, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Top applicants under product code HOM
Recent clearances under product code HOM
Data sourced from openFDA. This site is unofficial and independent of the FDA.