Cleared Special

K101694 - HANDHELD PULSE OXIMETER MODEL M800

K101694 is the FDA 510(k) clearance for HANDHELD PULSE OXIMETER MODEL M800 by Guangdong Biolight Meditech Co., Ltd.. It is a Class 2 Anesthesiology device (product code DQA) cleared through the Special 510(k) pathway after a 84-day FDA review.

K101694 · Guangdong Biolight Meditech Co., Ltd. · Anesthesiology device
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Sep 2010
Decision
84d
Days
Class 2
Risk

K101694 is an FDA 510(k) clearance for the HANDHELD PULSE OXIMETER MODEL M800. Classified as Oximeter (product code DQA), Class II - Special Controls.

Submitted by Guangdong Biolight Meditech Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on September 8, 2010 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 870.2700 - the FDA anesthesiology and respiratory device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Guangdong Biolight Meditech Co., Ltd. devices

Submission Details

510(k) Number K101694 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 16, 2010
Decision Date September 08, 2010
Days to Decision 84 days
Submission Type Special
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 140d · This submission: 84d
Pathway characteristics
Modification to existing cleared device.

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 369
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