Cleared Traditional

K953126 - OXILINK (SMALL, MEDIUM, LARGE)

K953126 is an FDA 510(k) clearance for OXILINK (SMALL, manufactured by Bci Intl., Inc.. The device is a Class 2 Anesthesiology device with product code DQA cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K953126 · Bci Intl., Inc. · Anesthesiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 1995
Decision
78d
Days
Class 2
Risk

K953126 is an FDA 510(k) clearance for the OXILINK (SMALL, MEDIUM, LARGE). Classified as Oximeter (product code DQA), Class II - Special Controls.

Submitted by Bci Intl., Inc. (Waukesha, US). The FDA issued a Cleared decision on September 21, 1995 after a review of 78 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 Bci Intl., Inc. devices

FDA 510(k) Submission Details - K953126

510(k) Number K953126 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 1995
Decision Date September 21, 1995
Days to Decision 78 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
62d faster than avg
Panel avg: 140d · This submission: 78d
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 686
Devices cleared under the same product code (DQA) and FDA review panel - the closest regulatory comparables to K953126.
BURDICK 200 PULSE OXIMETER
K954267 · Burdick, Inc. · May 1996
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K960251 · Aristo Medical Products, Inc. · Mar 1996
9267 SPO2 ATHENA MODULE
K940933 · S & W Medico Teknik · Nov 1995
NELLCOR SYMPHONY N-3000 PULSE OXIMETER
K952316 · Nellcor, Inc. · Aug 1995
NELLCOR N-20PA PORTABLE PULSE OXIMETER
K952222 · Nellcor, Inc. · Aug 1995
NEWOX2
K945754 · Bci Intl., Inc. · Jul 1995