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

iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C)

K Number: K223690 · Decision Dec 11, 2023
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
71
Applicant Total
1
Review Days
367

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Basic Information

Device Name
iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C)
K Number
K223690
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Yhlo Biotech Co., Ltd.
Date Received
December 9, 2022
Decision Date
December 11, 2023
Product Code
DHA
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
DHA System, Test, Human Chorionic Gonadotropin

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