EAJ — Apron, Leaded Class I

FDA Device Classification

FDA product code EAJ covers "Apron, Leaded", a Class I medical device regulated under 21 CFR 892.6500. Submissions are reviewed by the Radiology panel. At least 6 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EAJ
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
K931269bt medical coLEAD APRONJune 2, 1993
K913621rinn dental productsRINN PROTECTIVE X-RAY APRON AND PROTECTIVE COLLARSeptember 27, 1991
K870563x-techX-RAY APRONFebruary 19, 1987
K870103orthopedic systemsLEAD APRON CADDYJanuary 21, 1987
K832601e.m. adamsLEADED X-RAY APRONSeptember 29, 1983
K832602e.m. adamsTHYROID PROTECTIVE COLLARSeptember 29, 1983