KTAUnclassified

Medium, Contrast, Radiologic

Unknown

KTA is the FDA product code for Medium, Contrast, Radiologic. As of 2026-09-10, FDA records hold 8 510(k) clearances under this code, the most recent dated 1980-06-17, and no recalls.

Classification record

Product code: KTA
Device name: Medium, Contrast, Radiologic
Device class: Unclassified
Review panel: Unknown
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 8
Ingested recalls: 0

Clearances, product code KTA

By decision year

8 clearances under product code KTA with a decision year between 1976 and 1980, 1980 the highest year at 7.

Show the numbers

510(k) clearances under FDA product code KTA by decision year
Year	Clearances
1976	1
1980	7

Applicants with the most clearances

Product code KTA

Applicants holding the most 510(k) clearances under product code KTA
Applicant	Clearances
Medefield Pty., Ltd.	6
C.R. Bard Inc	1
Central Pharmaceuticals, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code KTA.

Recent clearances

Product code KTA

Recent recalls

Product code KTA

FDA records show no recalls under product code KTA.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)