Sysmex UF-100

FDA 510(k) K961054 · Sysmex Corp.

Substantially Equivalent

510(k) numberK961054

Submission

Device name
Sysmex UF-100
Applicant
Sysmex Corp.
Long Grove, IL, US
Received
March 18, 1996
Decision date
October 28, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LKM – Counter, Urine Particle
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5200
Specialty
Hematology

Other 510(k)s with product code LKM

510(k)DeviceApplicantDecision
K252580iQ200 SeriesLKM · Special Beckman Coulter, Inc.09/10/2025SE
K232416AUTION EYE AI-4510 Urine Particle Analysis SystemLKM · Traditional Arkray, Inc.05/03/2024SE
K210127iQ200 System, iChemVELOCITY Automated Urine Chemistry SystemLKM · Traditional Beckman Coulter, Inc.07/02/2021SE
K200811cobas u 701 microscopy analyzerLKM · Traditional Roche Diagnostics11/06/2020SE
K171883Sysmex UF-5000 Fully Automated Urine Particle AnalyzerLKM · Traditional Sysmex America, Inc.04/23/2018SE
K093861Iq 20 Series Analyzer, Iq 200 Series System, Nad Iq Lamina CradleLKM · Special Iris International, Inc.02/05/2010SE
K083002Sysmex UF-500I Automated Urine Particle AnalyzerLKM · Special Sysmex America, Inc.02/03/2009SE
K080887Sysmex UF-1000I, Automated Urine Particle Analyzer with Urinalysis Wam SoftwareLKM · Special Sysmex America, Inc.05/02/2008SE
K070910Sysmex Model UF1000ILKM · Traditional Sysmex America, Inc.05/25/2007SE
K053135Sysmex UF-100I Automated Urine Cell AnalyzerLKM · Traditional Sysmex America, Inc.01/04/2006SE

More from Sysmex America, Inc.

510(k)DeviceDecision
K012372Sysmex UF-50LKM · Traditional 09/28/2001SE
K992875Sysmex XE-2100, Automatated Hematology AnalyzerGKZ · Traditional 11/09/1999SE
K981950Sysmex R-3500, Automated Reticculocyte Analyzer, Model R-3500GKL · Traditional 11/03/1998SE
K981761Sysmex KX-21, Automated Hematology AnalyzerGKL · Traditional 08/14/1998SE
K971736Sysmex Immature Reticulocyte Fraction (Irf) ParameterGKZ · Traditional 08/26/1997SE
K964946Sysmex CA-1000/SYSMEX CA-5000JPA · Traditional 03/18/1997SE
K964375Sysmex SE/RAM-1GKL · Traditional 03/13/1997SE
K950508Sysmex SF-3000FPK · Traditional 11/03/1995SE
K945837Sysmex(Tm) F-820, 520GKZ · Traditional 06/09/1995SE
K942097Toa Medical Electronics CA-5000JPA · Traditional 03/24/1995SE

Questions and answers

When was Sysmex UF-100 cleared by the FDA?

Sysmex UF-100 (K961054) received a 510(k) decision of Substantially Equivalent on October 28, 1996, 224 days after the submission was received.

What is the product code of K961054?

The FDA product code is LKM – Counter, Urine Particle, a Class II (moderate risk) device regulated under 21 CFR 864.5200.