Cleared Traditional

K821488 - ELECATH PORTAL VEIN/BILIARY DRAIN ASSM

K821488 is an FDA 510(k) clearance for ELECATH PORTAL VEIN/BILIARY DRAIN ASSM, manufactured by Electro-Catheter Corp.. The device is a Class 1 Physical Medicine device with product code KNN cleared through the Traditional 510(k) pathway after a 10-day FDA review.

K821488 · Electro-Catheter Corp. · Physical Medicine device
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May 1982
Decision
10d
Days
Class 1
Risk

K821488 is an FDA 510(k) clearance for the ELECATH PORTAL VEIN/BILIARY DRAIN ASSM. Classified as Components, Wheelchair (product code KNN), Class I - General Controls.

Submitted by Electro-Catheter Corp. (Mchenry, US). The FDA issued a Cleared decision on May 28, 1982 after a review of 10 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3920 - the FDA physical medicine 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 Electro-Catheter Corp. devices

FDA 510(k) Submission Details - K821488

510(k) Number K821488 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 18, 1982
Decision Date May 28, 1982
Days to Decision 10 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
105d faster than avg
Panel avg: 115d · This submission: 10d
Pathway characteristics
Predicate-based equivalence.

KNN Device Classification - Class 1, General Controls

Product Code KNN Components, Wheelchair
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3920
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KNN Components, Wheelchair

All 11
Devices cleared under the same product code (KNN) and FDA review panel - the closest regulatory comparables to K821488.
WHEELCHAIR ACCESSORIES
K840629 · Poirier S.A. · Feb 1984
ARM THROUGH FOR WHEELCHAIR BK-6458-01
K823637 · Fred Sammons, Inc. · Jan 1983
ARM THROUGH FOR WHEELCHAIR BK 6454-01 &
K823638 · Fred Sammons, Inc. · Jan 1983
BK-6470 ADJUSTABLE ELEVATING WHEELCHAIR
K813636 · Fred Sammons, Inc. · Jan 1982
DESK ARM WHEELCHAIR ARM EXTENSION
K812348 · Fred Sammons, Inc. · Sep 1981
LEGREST, ELEVATING
K780192 · Orthopedic Equipment Co., Inc. · Feb 1978