Cleared Traditional

K810739 - SUCTION WOUND DRAINAGE DEVICE

K810739 is the FDA 510(k) clearance for SUCTION WOUND DRAINAGE DEVICE by The Urology Group. It is a Class 2 Gastroenterology & Urology device (product code KQT) cleared through the Traditional 510(k) pathway after a 99-day FDA review.

K810739 · The Urology Group · Gastroenterology & Urology device
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Jun 1981
Decision
99d
Days
Class 2
Risk

K810739 is an FDA 510(k) clearance for the SUCTION WOUND DRAINAGE DEVICE. Classified as Evacuator, Gastro-urology (product code KQT), Class II - Special Controls.

Submitted by The Urology Group (Mchenry, US). The FDA issued a Cleared decision on June 26, 1981 after a review of 99 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4370 - 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 The Urology Group devices

Submission Details

510(k) Number K810739 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 1981
Decision Date June 26, 1981
Days to Decision 99 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
31d faster than avg
Panel avg: 130d · This submission: 99d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KQT Evacuator, Gastro-urology
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4370
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 - KQT Evacuator, Gastro-urology

All 8
Devices cleared under the same product code (KQT) and FDA review panel - the closest regulatory comparables to K810739.
EVACUATOR, GASTRO-UROLOGY
K921451 · Northgate Technologies, Inc. · Oct 1992
VAN-TEC BLADDER EVACUATOR
K880099 · Van-Tec, Inc. · Mar 1988
DOSIMETRIC RELEASE
K830546 · American Hospital Supply Corp. · May 1983
CATHETER IRRIGATION SYRINGES, #3100,3110
K801781 · The Healthcare Group Laboratories, Inc. · Aug 1980
GENERAL PURPOSE IRRIGATING/ASPIR SYR.
K801782 · The Healthcare Group Laboratories, Inc. · Aug 1980
ELLIK BLADDER EVACUATOR
K800397 · Sage Products, Inc. · Mar 1980