Cleared Traditional

K100815 - OXIBLUE FINGERTIP PULSE OXIMETER MODEL ...

K100815 is an FDA 510(k) clearance for OXIBLUE FINGERTIP PULSE OXIMETER MODEL ..., manufactured by Oxypulse. The device is a Class 2 Anesthesiology device with product code DQA cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K100815 · Oxypulse · Anesthesiology device
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Jun 2010
Decision
85d
Days
Class 2
Risk

K100815 is an FDA 510(k) clearance for the OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE OXIM.... Classified as Oximeter (product code DQA), Class II - Special Controls.

Submitted by Oxypulse (Mesa, US). The FDA issued a Cleared decision on June 16, 2010 after a review of 85 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Oxypulse devices

FDA 510(k) Submission Details - K100815

510(k) Number K100815 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 23, 2010
Decision Date June 16, 2010
Days to Decision 85 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 140d · This submission: 85d
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 478
Devices cleared under the same product code (DQA) and FDA review panel - the closest regulatory comparables to K100815.
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K100617 · Masimo Corporation · May 2010
HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M
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