510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K864629Substantially Equivalent

Modified Dual Lumen Needle

Quinton, Inc., Seattle WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K864629 is the FDA 510(k) clearance record for MODIFIED DUAL LUMEN NEEDLE, a class II device, cleared for Quinton, Inc. on under FDA product code LBW (Set, Dialysis, Single Needle (Co-Axial Flow)). FDA records list 164 510(k) clearances for Quinton, Inc., from to . As of , FDA records show no recalls naming K864629.

Clearance record

Decision date
Received
(21 days to decision)
Product code
LBW Set, Dialysis, Single Needle (Co-Axial Flow)
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Quinton, Inc. 2121 Terry Ave., Seattle WA
Third party review
No

Clearances, product code LBW

Trailing 12 months

FDA records hold no clearances under product code LBW in the trailing twelve months.

FDA records show no clearances under product code LBW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LBW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260