IWT — Shield, Gonadal Class I

FDA Device Classification

FDA product code IWT covers "Shield, Gonadal", a Class I medical device regulated under 21 CFR 892.6500. 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
IWT
Device Class
Class I
Regulation Number
892.6500
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K930763byers industriesFIGLEAF SHIELDMay 17, 1993
K833523radiology designC.B. RADIOLOGY DESIGN GONADSHIELDNovember 21, 1983