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

Spo2 Sensor CSS032D

K Number: K251751 · Decision Dec 19, 2025
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
1
Review Days
193

Basic Information

Device Name
Spo2 Sensor CSS032D
K Number
K251751
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shenzhen Ykd Technology Co., Ltd.
Date Received
June 9, 2025
Decision Date
December 19, 2025
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DQA Oximeter

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