Product code HJC— Ophthalmic
ANESTHESIOMETER
- Classification name
- Esthesiometer, Ocular
- Device class
- Class 1
- Regulation
- 21 CFR 886.1040
- Advisory panel
- Ophthalmic
- Total cleared
- 2
- First cleared
- Most recent
Market context for product code HJC
FDA has cleared devices under product code HJC between 1985 and 1992, 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
- 1992
- 1985
Top applicants under product code HJC
Recent clearances under product code HJC
Data sourced from openFDA. This site is unofficial and independent of the FDA.