510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K103529Substantially Equivalent

Liaison Xl Analyzer Model 10050

Diasorin Inc., Stillwater MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K103529 is the FDA 510(k) clearance record for LIAISON XL ANALYZER MODEL 10050, a class II device, cleared for DiaSorin, Inc. on under FDA product code LOL (Hepatitis A Test (Antibody And Igm Antibody)). FDA records list 74 510(k) clearances for DiaSorin, Inc., from to . As of , FDA records show no recalls naming K103529.

Clearance record

Decision date
Received
(51 days to decision)
Product code
LOL Hepatitis A Test (Antibody And Igm Antibody)
Regulation
21 CFR 866.3310
Device class
Class II
Review panel
Microbiology
Applicant
DiaSorin, Inc. 195 Northwestern Ave., Stillwater MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LOL

Trailing 12 months
2 clearances under product code LOL 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 LOL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260