Cleared Traditional

K183277 - SpO2 Sensor

K183277 is the FDA 510(k) clearance for SpO2 Sensor by Shenzhen Upnmed Equipment Co., Ltd.. It is a Class 2 Anesthesiology device (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

Submission Details

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.

Device Classification

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 367
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