Product code LMA— Radiology

35/CD CINECONVERTER

Classification name
Digitizer, Image, Radiological
Device class
Class 2
Regulation
21 CFR 892.2030
Advisory panel
Radiology
Total cleared
61
First cleared
Most recent

Market context for product code LMA

FDA has cleared 61 devices under product code LMA between 1985 and 2013, filed by 38 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

last 15 years

Top applicants under product code LMA

Recent clearances under product code LMA

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