Product code EGY— Radiology

ALARA IMAGING SYSTEM

Classification name
Processor, Radiographic-Film, Automatic, Dental
Device class
Class 2
Regulation
21 CFR 892.1900
Advisory panel
Radiology
Total cleared
9
First cleared
Most recent

Market context for product code EGY

FDA has cleared 9 devices under product code EGY between 1977 and 1999, filed by 9 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code EGY

Recent clearances under product code EGY

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