FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Medconn 8K Glycated Hemoglobin Test System

K Number: K252749 · Decision Jan 6, 2026
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
25
Applicant Total
2
Review Days
130

Basic Information

Device Name
Medconn 8K Glycated Hemoglobin Test System
K Number
K252749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1373
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai Medconn Medical Technology Co., Ltd.
Date Received
August 29, 2025
Decision Date
January 6, 2026
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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Other Clearances by Shanghai Medconn Medical Technology Co., Ltd.

K Number Device Name
K242911 Medconn Glycated Hemoglobin Test system