510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K150304Substantially Equivalent

Oxyless Blood Tubing Set

Oxyless, Ltd., London, GB / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K150304 is the FDA 510(k) clearance record for Oxyless Blood Tubing Set, a class II device, cleared for Oxyless, Ltd. on under FDA product code FJK (Set, Tubing, Blood, With And Without Anti-Regurgitation Valve). FDA records list one 510(k) clearance for Oxyless, Ltd. As of , FDA records show no recalls naming K150304.

Clearance record

Decision date
Received
(383 days to decision)
Product code
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Oxyless, Ltd. Third Floor, Bewlay House, 2 Swallow Pl., London, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FJK

Trailing 12 months
2 clearances under product code FJK in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FJK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260