EGW — Dryer, Film, Radiographic Class II

FDA Device Classification

FDA product code EGW covers "Dryer, Film, Radiographic", a Class II medical device regulated under 21 CFR 892.1900. 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
EGW
Device Class
Class II
Regulation Number
892.1900
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K902531g-c intlEXAPHASE, SINGLE PHASE IMPRESSION MATERIALJuly 13, 1990
K760846pakoPAKOSTAT IIJanuary 7, 1977