Home / Device Classification / IXH

IXH — Camera, Focal Spot, Radiographic Class I

FDA Device Classification

FDA product code IXH covers "Camera, Focal Spot, Radiographic", a Class I medical device regulated under 21 CFR 892.1940. Submissions are reviewed by the Radiology panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
IXH
Device Class
Class I
Regulation Number
892.1940
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K023390mbf salesMY BREAST FRIEND, BREAST SELF-EXAM PADNovember 26, 2002
K851811victoreenSLIT CAMERA MODEL 07-624May 28, 1985

FDA data resources