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

Hipro Glycosylated Hemoglobin (HbA1c) Test System

K Number: K220999 · Decision Sep 12, 2024
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
25
Applicant Total
1
Review Days
892

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Basic Information

Device Name
Hipro Glycosylated Hemoglobin (HbA1c) Test System
K Number
K220999
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1373
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shijiazhuang Hipro Biotechnology Co., Ltd.
Date Received
April 4, 2022
Decision Date
September 12, 2024
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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