Cleared Traditional

K920780 - MEDSURG INSERTION TRAY

K920780 is an FDA 510(k) clearance for MEDSURG INSERTION TRAY, manufactured by Medsurg Industries, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code LFJ cleared through the Traditional 510(k) pathway after a 911-day FDA review.

K920780 · Medsurg Industries, Inc. · Gastroenterology & Urology device
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Aug 1994
Decision
911d
Days
Class 2
Risk

K920780 is an FDA 510(k) clearance for the MEDSURG INSERTION TRAY. Classified as Catheter, Subclavian (product code LFJ), Class II - Special Controls.

Submitted by Medsurg Industries, Inc. (Herndon, US). The FDA issued a Cleared decision on August 19, 1994 after a review of 911 days - an unusually long review period, suggesting complex equivalence evaluation.

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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Gastroenterology & Urology submissions.

View all Medsurg Industries, Inc. devices

FDA 510(k) Submission Details - K920780

510(k) Number K920780 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received February 20, 1992
Decision Date August 19, 1994
Days to Decision 911 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
780d slower than avg
Panel avg: 131d · This submission: 911d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LFJ Device Classification - Class 2, Special Controls

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 63
Devices cleared under the same product code (LFJ) and FDA review panel - the closest regulatory comparables to K920780.
AKCESS0CATH KIT
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SPLITTABLE SHEATH INTRODUCER SET
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COAXIAL ACUTE CATHETER
K931120 · Akcess Medical Products, Inc. · Jan 1994
VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERS
K914162 · Vas-Cath, Inc. · Jul 1993