DeviceClearance

Product code HMF— Ophthalmic

OPHTHALMIC STAND

Classification name
Stand, Instrument, Ac-Powered, Ophthalmic
Device class
Class 1
Regulation
21 CFR 886.1860
Advisory panel
Ophthalmic
Total cleared
15
First cleared
Most recent

Market context for product code HMF

FDA has cleared 15 devices under product code HMF between 1979 and 1994, filed by 11 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

Top applicants under product code HMF

Recent clearances under product code HMF

Data sourced from openFDA. This site is unofficial and independent of the FDA.