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

Pulse Oximeter

K Number: K211400 · Decision Feb 11, 2022
Classifications
1
FEI Numbers
403
Registration Numbers
403
Same Product Code
711
Applicant Total
10
Review Days
282

Basic Information

Device Name
Pulse Oximeter
K Number
K211400
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beijing Choice Electronic Technology Co., Ltd.
Date Received
May 5, 2021
Decision Date
February 11, 2022
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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