Cleared Traditional

K832143 - MARK III OXYGEN WALKER SYS. RESERVOIR

K832143 is an FDA 510(k) clearance for MARK III OXYGEN WALKER SYS. RESERVOIR, manufactured by Linde Div. Union Carbide Corp.. The device is a Class 2 Anesthesiology device with product code BYJ cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K832143 · Linde Div. Union Carbide Corp. · Anesthesiology device
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Aug 1983
Decision
52d
Days
Class 2
Risk

K832143 is an FDA 510(k) clearance for the MARK III OXYGEN WALKER SYS. RESERVOIR. Classified as Unit, Liquid-oxygen, Portable (product code BYJ), Class II - Special Controls.

Submitted by Linde Div. Union Carbide Corp. (Mchenry, US). The FDA issued a Cleared decision on August 26, 1983 after a review of 52 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5655 - 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 Linde Div. Union Carbide Corp. devices

FDA 510(k) Submission Details - K832143

510(k) Number K832143 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 1983
Decision Date August 26, 1983
Days to Decision 52 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 140d · This submission: 52d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BYJ Device Classification - Class 2, Special Controls

Product Code BYJ Unit, Liquid-oxygen, Portable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5655
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 - BYJ Unit, Liquid-oxygen, Portable

All 18
Devices cleared under the same product code (BYJ) and FDA review panel - the closest regulatory comparables to K832143.
PURITAN-BENNETT COMPANION EMT LIQUID OXYGEN
K895387 · Puritan Bennett Corp. · Jan 1990
COMPANION LIQUID OXYGEN SYSTEM
K861503 · Puritan Bennett Corp. · Jun 1986
MARK 4 LIQUID OXYGEN SYSTEM
K860937 · Puritan Bennett Corp. · Mar 1986
MARK III OXYGEN WALKER SYS-LOW PRESS
K830337 · Union Carbide Corp. · Mar 1983
LIQUID OXYGEN SYSTEM
K830498 · Puritan Bennett Corp. · Mar 1983
MARK III OXYGEN WALKER SYSTEM
K820836 · Union Carbide Corp. · Apr 1982