DeviceClearance

Product code IZD— Radiology

ACCUSPEC THYROID UPTAKE SYSTEM

Classification name
Probe, Uptake, Nuclear
Device class
Class 1
Regulation
21 CFR 892.1320
Advisory panel
Radiology
Total cleared
30
First cleared
Most recent

Market context for product code IZD

FDA has cleared 30 devices under product code IZD between 1976 and 2014, filed by 15 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 IZD

Recent clearances under product code IZD

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