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

AViTA Pulse Oximeter (SP61)

K Number: K252448 · Decision Feb 27, 2026
Classifications
1
FEI Numbers
400
Registration Numbers
400
Same Product Code
725
Applicant Total
27
Review Days
207

Basic Information

Device Name
AViTA Pulse Oximeter (SP61)
K Number
K252448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Avita Corporation
Date Received
August 4, 2025
Decision Date
February 27, 2026
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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