DeviceClearance

Product code HNF— Ophthalmic

13-550,13-560 WESCOTT SCOSSORS (EYE)

Classification name
Scissors, Ophthalmic
Device class
Class 1
Regulation
21 CFR 886.4350
Advisory panel
Ophthalmic
Total cleared
15
First cleared
Most recent

Market context for product code HNF

FDA has cleared 15 devices under product code HNF between 1976 and 2002, filed by 10 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 HNF

Recent clearances under product code HNF

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