510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
IXFClass I

Test-Pattern, Radiographic

21 CFR 892.1940 / Radiology
FDA source (opens on fda.gov)

IXF is the FDA product code for Test-Pattern, Radiographic, a class I device type, regulated under 21 CFR 892.1940. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IXF
Device name
Test-Pattern, Radiographic
Regulation
21 CFR 892.1940
Device class
Class I
Review panel
Radiology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
5
Ingested recalls
0

Clearances, product code IXF

By decision year
5 clearances under product code IXF with a decision year between 1981 and 1987, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code IXF by decision year
YearClearances
19811
19842
19851
19871

Applicants with the most clearances

Product code IXF
Applicants holding the most 510(k) clearances under product code IXF
ApplicantClearances
Radiation Measurements, Inc.2
Computerized Imaging Reference Systems, Inc.1
Machlett Laboratories, Inc.1
Victoreen, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order