Cleared Traditional

K882468 - ELIMINATOR AIR FILTER

K882468 is the FDA 510(k) clearance for ELIMINATOR AIR FILTER by Apex Medical, Inc.. It is a Class 2 General Hospital device (product code KDQ) cleared through the Traditional 510(k) pathway after a 75-day FDA review.

K882468 · Apex Medical, Inc. · General Hospital
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Aug 1988
Decision
75d
Days
Class 2
Risk

K882468 is an FDA 510(k) clearance for the ELIMINATOR AIR FILTER. Classified as Bottle, Collection, Vacuum (product code KDQ), Class II - Special Controls.

Submitted by Apex Medical, Inc. (Martinsville, US). The FDA issued a Cleared decision on August 29, 1988 after a review of 75 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6740 - the FDA general hospital 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 Apex Medical, Inc. devices

Submission Details

510(k) Number K882468 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 15, 1988
Decision Date August 29, 1988
Days to Decision 75 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
54d faster than avg
Panel avg: 129d · This submission: 75d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KDQ Bottle, Collection, Vacuum
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6740
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 General Hospital devices follow this clearance model.

Regulatory Peers - KDQ Bottle, Collection, Vacuum

All 31
Devices cleared under the same product code (KDQ) and FDA review panel - the closest regulatory comparables to K882468.
PLEUR-EVAC(R) A-6020--INFANT SINGLE USE CHEST DRAI
K896697 · Deknatel, Inc. · Feb 1990
THORA-KLEX CHEST DRAINAGE UNIT
K896127 · Davol, Inc. · Jan 1990
PLEUR-EVAC A-8002--ADULT/PEDIATRIC DUAL COLLECTION
K892915 · Deknatel, Inc. · Jun 1989
PLEUR-EVAC-A-7000--ADULT/PEDI CHEST DRAINAGE SYST
K882223 · Deknatel, Inc. · Aug 1988
MUCUS TRAP OR SUCTION TRAP
K881149 · Ferguson Medical · Jun 1988
URESIL THORACIC VENT
K863561 · Uresil Corp. · Sep 1986