KPZ — Generator, High Voltage, X-Ray, Therapeutic Class II

FDA Device Classification

FDA product code KPZ covers "Generator, High Voltage, X-Ray, Therapeutic", a Class II medical device regulated under 21 CFR 892.5900. Submissions are reviewed by the Radiology panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
KPZ
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
K912249theta systemsPATIENT DOSE MONITORAugust 30, 1991
K860469victoreen37-701-1 PATIENT DOASE MONITOR WITH DETECTORSApril 16, 1986
K854410old delft corp. of americaVERIFLEXFebruary 12, 1986