EGY — Processor, Radiographic-Film, Automatic, Dental Class II

FDA Device Classification

FDA product code EGY covers "Processor, Radiographic-Film, Automatic, Dental", a Class II medical device regulated under 21 CFR 892.1900. Submissions are reviewed by the Radiology panel. At least 9 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EGY
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
K992896dental x-ray support systemsDXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)September 3, 1999
K955825smith companies dental productsSMITH S-100 TIME & TEMPERATURE CONTROLApril 5, 1996
K955643denoptixALARA IMAGING SYSTEMMarch 1, 1996
K945682gendexPROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTALFebruary 9, 1995
K900156allied photo products coAP201 DENTAL X-RAY FILM PROCESSORMay 14, 1990
K874118dent-xMODEL 410 DENTAL X-RAY FILM PROCESSORSNovember 6, 1987
K811211kaycor intlYOSHIDA AP 100June 16, 1981
K771433ada products coAUTO. DEVEL. UNIT FOO DENTAL X-RAYAugust 19, 1977
K770783general electricFILM PROCESSOR, AUTOMATICMay 10, 1977