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

Table, Radiographic, Stationary Top

21 CFR 892.1980 / Radiology
FDA source (opens on fda.gov)

IXQ is the FDA product code for Table, Radiographic, Stationary Top, a class II device type, regulated under 21 CFR 892.1980. As of , FDA records hold 27 510(k) clearances under this code, the most recent dated , and 7 recalls.

Classification record

Product code
IXQ
Device name
Table, Radiographic, Stationary Top
Regulation
21 CFR 892.1980
Device class
Class II
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
27
Ingested recalls
7

Clearances, product code IXQ

By decision year
27 clearances under product code IXQ with a decision year between 1978 and 1997, 1992 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code IXQ by decision year
YearClearances
19783
19841
19852
19863
19871
19881
19892
19903
19911
19924
19942
19952
19961
19971

Applicants with the most clearances

Product code IXQ
Applicants holding the most 510(k) clearances under product code IXQ
ApplicantClearances
Atomic Products Corp.2
Continental X-Ray Corp.2
Garrels X-Ray Products, Inc.2
Medtec LLC2
Tecnomed, Inc.2
Altairex Manufacturing, Inc.1
Brattle Instrument Corp.1
Carolina X-Ray Co., Inc.1
Dial-A-Rad1
Hofmann X-Ray of America, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 22 companies shown, in name order