Product code IXC— Radiology
ADVIEWER 2000
- Classification name
- Illuminator, Radiographic-Film
- Device class
- Class 1
- Regulation
- 21 CFR 892.1890
- Advisory panel
- Radiology
- Total cleared
- 18
- First cleared
- Most recent
Market context for product code IXC
FDA has cleared devices under product code IXC between 1980 and 1999, filed by 16 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1999
- 1997
- 1996
- 1995
- 1992
- 1988
- 1987
- 1986
- 1984
- 1981
- 1980
Top applicants under product code IXC
Recent clearances under product code IXC
- K991302 — SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUS
- K973965 — SMART MOTORIZED VIEWER
- K973115 — ARRIPRO 35 ST/TV
- K970240 — DIFFUSER PANEL
- K954998 — LILY DARK VIEWER
- K954199 — VOXBOX
- K952188 — ADVIEWER 2000
- K922848 — ULTRALITE X-RAY FILM ILLUMINATOR
- K922079 — ROTOLUX, SELECTOLUX, SHUTTERVUE
- K883702 — EXCELVIEW ILLUMINATOR
- K875233 — VARIVIEWER (X-RAY FILM VIEWER)
- K872245 — PROVIEW (E7015) & PROLINK IMAGE DISPLAY SYSTEM
- K854933 — SANDHILL ELECTRONIC CALIPER
- K840607 — LF MOTORIZED RADIOGRAPHIC FILM VIEWER
- K812152 — MEDI VIEW
- K802215 — VIEW-LITE, MODEL-S
- K802216 — VIEW-LITE, MODEL-DL
- K802217 — VIEW-LITE, MODEL-SL
Data sourced from openFDA. This site is unofficial and independent of the FDA.