Product code HLP— Ophthalmic

THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.

Classification name
Target, Fusion And Stereoscopic
Device class
Class 1
Regulation
21 CFR 886.1880
Advisory panel
Ophthalmic
Total cleared
3
First cleared
Most recent

Market context for product code HLP

FDA has cleared 3 devices under product code HLP, all in 1988, 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.

Top applicants under product code HLP

Recent clearances under product code HLP

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