Product code HOB— Ophthalmic
CATEGORY 6 OPTHALMIC DEVICES
- Classification name
- Clamp, Muscle, Ophthalmic
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code HOB
FDA has cleared devices under product code HOB between 1978 and 1984, filed by 3 applicant companies. 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.
Clearances per year
- 1984
- 1978
Top applicants under product code HOB
Recent clearances under product code HOB
Data sourced from openFDA. This site is unofficial and independent of the FDA.