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

Phantom, Anthropomorphic, Radiographic

21 CFR 892.1950 / Radiology
FDA source (opens on fda.gov)

IXG is the FDA product code for Phantom, Anthropomorphic, Radiographic, a class I device type, regulated under 21 CFR 892.1950. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IXG
Device name
Phantom, Anthropomorphic, Radiographic
Regulation
21 CFR 892.1950
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
4
Ingested recalls
0

Clearances, product code IXG

By decision year
4 clearances under product code IXG with a decision year between 1984 and 1991, 1984 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code IXG by decision year
YearClearances
19842
19851
19911

Applicants with the most clearances

Product code IXG
Applicants holding the most 510(k) clearances under product code IXG
ApplicantClearances
Bennett X-Ray Corp.1
Cirs, Inc.1
Computerized Imaging Reference Systems, Inc.1
Imatron, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 19 companies shown, in name order