Cleared Traditional

K880262 - MOBILE PAK, MODEL DC

K880262 is an FDA 510(k) clearance for MOBILE PAK, manufactured by Intl. Biomedical Concepts, Inc.. The device is a Class 2 Anesthesiology device with product code CAW cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K880262 · Intl. Biomedical Concepts, Inc. · Anesthesiology device
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Feb 1988
Decision
21d
Days
Class 2
Risk

K880262 is an FDA 510(k) clearance for the MOBILE PAK, MODEL DC. Classified as Generator, Oxygen, Portable within the CAW classification (a category for home-use oxygen therapy and respiratory devices), Class II - Special Controls.

Submitted by Intl. Biomedical Concepts, Inc. (Englewood, US). The FDA issued a Cleared decision on February 12, 1988 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5440 - 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.

FDA 510(k) Submission Details - K880262

510(k) Number K880262 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 1988
Decision Date February 12, 1988
Days to Decision 21 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
119d faster than avg
Panel avg: 140d · This submission: 21d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CAW Device Classification - Class 2, Special Controls

Product Code CAW Generator, Oxygen, Portable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5440
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 - CAW Generator, Oxygen, Portable

All 233
Devices cleared under the same product code (CAW) and FDA review panel - the closest regulatory comparables to K880262.
RELIANT OXYGEN CONCENTRATOR
K884581 · Airsep Corp. · Jan 1989
PORTABLE OXYGEN GENERATOR
K884084 · Mountain Medical Equipment, Inc. · Nov 1988
ALPINE PORTABLE OXYGEN GENERATOR
K881802 · Mountain Medical Equipment, Inc. · Jul 1988
4LYF OXYGEN CONCENTRATOR
K872534 · Airsep Corp. · Oct 1987
BUNN CONCENTRATOR MODEL 2100 SERIES
K873071 · The John Bunn Co. · Sep 1987
CRITERION II & IIA OXYGEN CONCENTRATORS
K871603 · Timeter Instrument Corp. · Aug 1987
K880262 · MOBILE PAK, MODEL DC
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