Cleared Traditional

K881149 - MUCUS TRAP OR SUCTION TRAP

K881149 is the FDA 510(k) clearance for MUCUS TRAP OR SUCTION TRAP by Ferguson Medical. It is a Class 2 General Hospital device (product code KDQ) cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K881149 · Ferguson Medical · General Hospital
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Jun 1988
Decision
89d
Days
Class 2
Risk

K881149 is an FDA 510(k) clearance for the MUCUS TRAP OR SUCTION TRAP. Classified as Bottle, Collection, Vacuum (product code KDQ), Class II - Special Controls.

Submitted by Ferguson Medical (Chico, US). The FDA issued a Cleared decision on June 14, 1988 after a review of 89 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 Ferguson Medical devices

Submission Details

510(k) Number K881149 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 17, 1988
Decision Date June 14, 1988
Days to Decision 89 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 129d · This submission: 89d
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 32
Devices cleared under the same product code (KDQ) and FDA review panel - the closest regulatory comparables to K881149.
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
URESIL THORACIC VENT
K863561 · Uresil Corp. · Sep 1986
T-VAC PLEURAL DRAINAGE UNIT, 7800 SERIES
K861025 · Boehringer Laboratories · Apr 1986
FILTERED VACUUM SAFETY TRAP BOTTLE
K855074 · Boehringer Laboratories · Mar 1986