Product code IXJ— Radiology
RADIOGRAPHIC GRID
- Classification name
- Grid, Radiographic
- Device class
- Class 1
- Regulation
- 21 CFR 892.1910
- Advisory panel
- Radiology
- Total cleared
- 15
- First cleared
- Most recent
Market context for product code IXJ
FDA has cleared devices under product code IXJ between 1983 and 1997, filed by 15 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
- 1997
- 1996
- 1995
- 1994
- 1993
- 1992
- 1990
- 1988
- 1986
- 1983
Top applicants under product code IXJ
Recent clearances under product code IXJ
- K964025 — MITAYA ALUMINUM INTERSPACED X-RAY GRID
- K963893 — FIBRE INTERSPACED X-RAY GRID
- K962338 — RADIOGRAPHIC GRID
- K954294 — HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZES
- K945697 — SK S-RAY GRIDS
- K945327 — JPI X-RAY GRID
- K941626 — GRIDGIL
- K940309 — X-RAY GRID (RADIOLOGICAL GRID)
- K926445 — SOYEE ALUMINUM INTERSPACED X-RAY GRID
- K926261 — JPI ALUMINUM INTERSPACED X-RAY GRID
- K925997 — KODAK EKTASCAN SP CASSETTE
- K901012 — RADIOGRAPHIC GRID
- K883527 — GRID/RADIOGRAPHIC
- K854459 — TBX MEDICAL X-RAY TABLE
- K837776 — AOR X-RAY ALIGMENT PAD
Data sourced from openFDA. This site is unofficial and independent of the FDA.