Cleared Traditional

K183277 - SpO2 Sensor

K183277 is an FDA 510(k) clearance for SpO2 Sensor, manufactured by Shenzhen Upnmed Equipment Co., Ltd.. The device is a Class 2 Anesthesiology device with product code DQA cleared through the Traditional 510(k) pathway after a 173-day FDA review.

K183277 · Shenzhen Upnmed Equipment Co., Ltd. · Anesthesiology device
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May 2019
Decision
173d
Days
Class 2
Risk

K183277 is an FDA 510(k) clearance for the SpO2 Sensor. Classified as Oximeter (product code DQA), Class II - Special Controls.

Submitted by Shenzhen Upnmed Equipment Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on May 15, 2019 after a review of 173 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 870.2700 - the FDA anesthesiology and respiratory device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Shenzhen Upnmed Equipment Co., Ltd. devices

FDA 510(k) Submission Details - K183277

510(k) Number K183277 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 23, 2018
Decision Date May 15, 2019
Days to Decision 173 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
33d slower than avg
Panel avg: 140d · This submission: 173d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQA Device Classification - Class 2, Special Controls

Product Code DQA Oximeter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2700
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Anesthesiology devices follow this clearance model.

Regulatory Peers - DQA Oximeter

All 577
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