FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01

K Number: K250073 · Decision Oct 3, 2025
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
25
Applicant Total
20
Review Days
266

Basic Information

Device Name
Tosoh Automated Glycohemoglobin Analyzer HLC-723GR01
K Number
K250073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1373
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tosoh Bioscience, Inc.
Date Received
January 10, 2025
Decision Date
October 3, 2025
Product Code
PDJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PDJ Hemoglobin A1c Test System

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