Cleared Traditional

K821954 - MCSCK838 CATHETER IN A TRAY (KIT)

K821954 is the FDA 510(k) clearance for MCSCK838 CATHETER IN A TRAY (KIT) by Medcomp. It is a Class 2 Gastroenterology & Urology device (product code LFJ) cleared through the Traditional 510(k) pathway after a 14-day FDA review.

K821954 · Medcomp · Gastroenterology & Urology device
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Jul 1982
Decision
14d
Days
Class 2
Risk

K821954 is an FDA 510(k) clearance for the MCSCK838 CATHETER IN A TRAY (KIT). Classified as Catheter, Subclavian (product code LFJ), Class II - Special Controls.

Submitted by Medcomp (Mchenry, US). The FDA issued a Cleared decision on July 14, 1982 after a review of 14 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5540 - the FDA gastroenterology and urology 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 Medcomp devices

Submission Details

510(k) Number K821954 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 30, 1982
Decision Date July 14, 1982
Days to Decision 14 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
116d faster than avg
Panel avg: 130d · This submission: 14d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code LFJ Catheter, Subclavian
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5540
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - LFJ Catheter, Subclavian

All 23
Devices cleared under the same product code (LFJ) and FDA review panel - the closest regulatory comparables to K821954.
RIGHT ATRIAL CATHETER
K822964 · Quinton, Inc. · Nov 1982
RIGHT ARTERIAL CATHETER
K822910 · Quinton, Inc. · Nov 1982
SHIELY DUEL LUMEN SUBCLAVIAN CANNULA
K822134 · Shiley, Inc. · Aug 1982
MAHURKAR SUBCLAVIAN CATHETER
K821400 · Quinton, Inc. · Jun 1982
COBE ACUFLEX SSN, #15-220
K820238 · Cobe Laboratories, Inc. · Mar 1982
SORENSON SUBCLAVIAN CATHETER SSC-8
K812326 · Sorensen Research · Sep 1981