510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K233875Substantially Equivalent

Brainomix 360 e-Lung

Brainomix Limited, Oxford, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K233875 is the FDA 510(k) clearance record for Brainomix 360 e-Lung, a class II device, cleared for Brainomix Limited on under FDA product code JAK (System, X-Ray, Tomography, Computed). FDA records list 13 510(k) clearances for Brainomix Limited, from to . As of , FDA records show no recalls naming K233875.

Clearance record

Decision date
Received
(158 days to decision)
Product code
JAK System, X-Ray, Tomography, Computed
Regulation
21 CFR 892.1750
Device class
Class II
Review panel
Radiology
Applicant
Brainomix Limited First Floor, Seacourt Tower, Oxford, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JAK

Trailing 12 months
20 clearances under product code JAK in the twelve months to October 2026, March 2026 the highest month at 10.
Show the numbers
Monthly 510(k) clearances under FDA product code JAK, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 202610
April 20260
May 20261
June 20262
July 20262
August 20260
September 20263
October 20260