Product code HOC— Ophthalmic
PART #860070 ULTRAPAK & #860075 ULTRAPAK
- Classification name
- Clip, Iris Retractor
- Device class
- Class 1
- Regulation
- 21 CFR 886.4350
- Advisory panel
- Ophthalmic
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code HOC
FDA has cleared devices under product code HOC between 1983 and 1987, filed by 2 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
- 1987
- 1983
Top applicants under product code HOC
Recent clearances under product code HOC
Data sourced from openFDA. This site is unofficial and independent of the FDA.