510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K951005Substantially Equivalent

Kenex Injector Head Support (as Exhibit 2)

Kenex, Ltd., England, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951005 is the FDA 510(k) clearance record for KENEX INJECTOR HEAD SUPPORT (AS EXHIBIT 2), a class II device, cleared for Kenex , Ltd. on under FDA product code IZQ (Injector, Contrast Medium, Automatic). FDA records list 3 510(k) clearances for Kenex , Ltd., from to . As of , FDA records show no recalls naming K951005.

Clearance record

Decision date
Received
(78 days to decision)
Product code
IZQ Injector, Contrast Medium, Automatic
Regulation
21 CFR 870.1650
Device class
Class II
Review panel
Cardiovascular
Applicant
Kenex , Ltd. Langley House 24 Burnt Mill, England, GB
510(k) summary
Summary
Third party review
No

Clearances, product code IZQ

Trailing 12 months
3 clearances under product code IZQ in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IZQ, trailing twelve months
MonthClearances
November 20252
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260