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SYSMEX UF-100

K961054 Class II Traditional
Decision Date
1996-10-28
Sponsor / Applicant
Sysmex Corp.

Technical Specification

510(k) Submission ID K961054
Product Code LKM
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5200
Decision Date 1996-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSMEX UF-100 received FDA 510(k) clearance under submission number K961054, sponsored by Sysmex Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1996-10-28.

Classification & Regulation

This clearance is catalogued under FDA product code LKM and 21 CFR 864.5200, within the Hematology review panel as a Class II device.