Product code HPT— Ophthalmic

AUTO PERIOMETER 3000

Classification name
Perimeter, Automatic, Ac-Powered
Device class
Class 1
Regulation
21 CFR 886.1605
Advisory panel
Ophthalmic
Total cleared
41
First cleared
Most recent

Market context for product code HPT

FDA has cleared 41 devices under product code HPT between 1978 and 2010, filed by 30 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

last 15 years

Top applicants under product code HPT

Recent clearances under product code HPT

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