Product code IYP— Radiology

LINEAR SCANNER PROBE ELSCINT LTD. TL-35

Classification name
Phantom, Anthropomorphic, Nuclear
Device class
Class 1
Regulation
21 CFR 892.1370
Advisory panel
Radiology
Total cleared
3
First cleared
Most recent

Market context for product code IYP

FDA has cleared 3 devices under product code IYP between 1981 and 1992, 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 IYP

Recent clearances under product code IYP

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