IYD — Generator, Low Voltage, Therapeutic X-Ray Class II

FDA Device Classification

FDA product code IYD covers "Generator, Low Voltage, Therapeutic X-Ray", a Class II medical device regulated under 21 CFR 892.5900. Submissions are reviewed by the Radiology panel. At least 1 recent 510(k) clearance has been granted under this product code.

Classification Details

Product Code
IYD
Device Class
Class II
Regulation Number
892.5900
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K914583toshiba america medical systems, in.cTOSBEEJanuary 28, 1993