Cleared Traditional

K992941 - LEMAITRE BILIARY CATHETER

K992941 is an FDA 510(k) clearance for LEMAITRE BILIARY CATHETER, manufactured by Vascutech, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code LQR cleared through the Traditional 510(k) pathway after a 134-day FDA review.

K992941 · Vascutech, Inc. · Gastroenterology & Urology device
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Jan 2000
Decision
134d
Days
Class 2
Risk

K992941 is an FDA 510(k) clearance for the LEMAITRE BILIARY CATHETER. Classified as Dislodger, Stone, Biliary (product code LQR), Class II - Special Controls.

Submitted by Vascutech, Inc. (Burlington, US). The FDA issued a Cleared decision on January 12, 2000 after a review of 134 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5010 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Vascutech, Inc. devices

FDA 510(k) Submission Details - K992941

510(k) Number K992941 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1999
Decision Date January 12, 2000
Days to Decision 134 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
4d slower than avg
Panel avg: 130d · This submission: 134d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LQR Device Classification - Class 2, Special Controls

Product Code LQR Dislodger, Stone, Biliary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5010
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 - LQR Dislodger, Stone, Biliary

All 26
Devices cleared under the same product code (LQR) and FDA review panel - the closest regulatory comparables to K992941.
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