510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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IXCClass I

Illuminator, Radiographic-Film

21 CFR 892.1890 / Radiology
FDA source (opens on fda.gov)

IXC is the FDA product code for Illuminator, Radiographic-Film, a class I device type, regulated under 21 CFR 892.1890. As of , FDA records hold 18 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IXC
Device name
Illuminator, Radiographic-Film
Regulation
21 CFR 892.1890
Device class
Class I
Review panel
Radiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
18
Ingested recalls
0

Clearances, product code IXC

By decision year
18 clearances under product code IXC with a decision year between 1980 and 1999, 1980 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code IXC by decision year
YearClearances
19803
19811
19841
19861
19871
19882
19922
19952
19961
19973
19991

Applicants with the most clearances

Product code IXC
Applicants holding the most 510(k) clearances under product code IXC
ApplicantClearances
Med-Western Electronics, Inc.3
Smartlight, Inc.2
A & S Trading Co.1
Adp, Ltd.1
American Medical Sales, Inc.1
Arnold & Richter Cine Technik1
Diversified Diagnostic Products, Inc.1
Excel Medical Products, Inc.1
Focused Viewer, Inc.1
General Electric Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 18 companies shown, in name order