Cleared Traditional

AViTA Pulse Oximeter

K223399 · Avita Corporation · Anesthesiology
May 2024
Decision
558d
Days
Class 2
Risk

About This 510(k) Submission

K223399 is an FDA 510(k) clearance for the AViTA Pulse Oximeter, a Oximeter (Class II — Special Controls, product code DQA), submitted by Avita Corporation (New Taipei City, TW). The FDA issued a Cleared decision on May 20, 2024, 558 days after receiving the submission on November 9, 2022. This device falls under the Anesthesiology review panel. Regulated under 21 CFR 870.2700.

Submission Details

510(k) Number K223399 FDA.gov
FDA Decision Cleared SESE
Date Received November 09, 2022
Decision Date May 20, 2024
Days to Decision 558 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF

Device Classification

Product Code DQA — Oximeter
Device Class Class II — Special Controls
CFR Regulation 21 CFR 870.2700

Similar Devices — DQA Oximeter

All 721
AViTA Pulse Oximeter (SP61)
K252448 · Avita Corporation · Feb 2026
YUWELL? Finger Pulse Oximeter (YX105, YX106, YX110, YX310)
K252805 · Jiangsu Yuyue Medical Equipment& Supply Co., Ltd. · Feb 2026
Reusable SPO2 Sensor (BSA307-47; BSA109-50; BSA109-31O)
K253109 · Shenzhen Best Electronics Co., Ltd. · Jan 2026
Spo2 Sensor CSS032D
K251751 · Shenzhen Ykd Technology Co., Ltd. · Dec 2025
Unimed Reusable SpO2 Sensors (-08 Series) (U403S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U203S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U103S-08); Unimed Reusable SpO2 Sensors (-08 Series) (U103-08)
K251691 · Unimed Medical Supplies, Inc. · Dec 2025
Unimed Reusable SpO2 Sensors (-48 Series and -29 Series) (U410-48); Unimed Reusable SpO2 Sensors (-48 Series and -29 Series) (U410-29)
K251696 · Unimed Medical Supplies, Inc. · Dec 2025