IXC — Illuminator, Radiographic-Film Class I

FDA Device Classification

FDA product code IXC covers "Illuminator, Radiographic-Film", a Class I medical device regulated under 21 CFR 892.1890. Submissions are reviewed by the Radiology panel. At least 18 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
IXC
Device Class
Class I
Regulation Number
892.1890
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K991302smartlightSMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUSJune 1, 1999
K973965smartlightSMART MOTORIZED VIEWERDecember 12, 1997
K973115arnold and richter cine technikARRIPRO 35 ST/TVSeptember 2, 1997
K970240focused viewerDIFFUSER PANELMarch 11, 1997
K954998lily imaging solutionsLILY DARK VIEWERJanuary 29, 1996
K954199voxelVOXBOXSeptember 29, 1995
K952188adpADVIEWER 2000May 30, 1995
K922848a and s tradingULTRALITE X-RAY FILM ILLUMINATORSeptember 28, 1992
K922079american medical salesROTOLUX, SELECTOLUX, SHUTTERVUEJune 16, 1992
K883702excel medical productsEXCELVIEW ILLUMINATORSeptember 19, 1988
K875233diversified diagnostic productsVARIVIEWER (X-RAY FILM VIEWER)January 19, 1988
K872245general electricPROVIEW (E7015) & PROLINK IMAGE DISPLAY SYSTEMJune 19, 1987
K854933sandhillSANDHILL ELECTRONIC CALIPERFebruary 12, 1986
K840607sybronLF MOTORIZED RADIOGRAPHIC FILM VIEWERMarch 5, 1984
K812152medical synergyMEDI VIEWSeptember 9, 1981
K802217med-western electronicsVIEW-LITE, MODEL-SLOctober 23, 1980
K802216med-western electronicsVIEW-LITE, MODEL-DLOctober 23, 1980
K802215med-western electronicsVIEW-LITE, MODEL-SOctober 23, 1980