Product code HCD— Neurology

Alcyone MEMS Cannula (AMC) System

Classification name
Cannula, Ventricular
Device class
Class 1
Regulation
21 CFR 882.4060
Advisory panel
Neurology
Total cleared
3
First cleared
Most recent

Market context for product code HCD

FDA has cleared 3 devices under product code HCD between 1992 and 2015, filed by 3 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 HCD

Recent clearances under product code HCD

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