Cleared Traditional

K871999 - MMG URO-SELF CATHETER

K871999 is an FDA 510(k) clearance for MMG URO-SELF CATHETER, manufactured by Medical Marketing Group. The device is a Class 2 Gastroenterology & Urology device with product code GBM cleared through the Traditional 510(k) pathway after a 91-day FDA review.

K871999 · Medical Marketing Group · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1987
Decision
91d
Days
Class 2
Risk

K871999 is an FDA 510(k) clearance for the MMG URO-SELF CATHETER. Classified as Catheter, Urethral (product code GBM), Class II - Special Controls.

Submitted by Medical Marketing Group (Decatur, US). The FDA issued a Cleared decision on August 25, 1987 after a review of 91 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5130 - 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 Medical Marketing Group devices

FDA 510(k) Submission Details - K871999

510(k) Number K871999 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 1987
Decision Date August 25, 1987
Days to Decision 91 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
40d faster than avg
Panel avg: 131d · This submission: 91d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GBM Device Classification - Class 2, Special Controls

Product Code GBM Catheter, Urethral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5130
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 - GBM Catheter, Urethral

All 65
Devices cleared under the same product code (GBM) and FDA review panel - the closest regulatory comparables to K871999.
AUTOCATH(TM) SET
K910876 · Cook Urological, Inc. · May 1991
KENDALL CURITY URETHRAL CATHETERS
K892442 · The Kendal Co. · Jun 1989
KENDALL CURITY & KENGUARD RED RUBBER URETHRAL CATH
K881667 · The Kendal Co. · Aug 1988
OPEN ENDED URETERAL CATHETER
K830840 · Van-Tec, Inc. · Apr 1983
CATHETER, SILICONE FOLEY (BARDEX)
K760093 · C.R. Bard, Inc. · Aug 1976
TRAY, UNIVERSAL FOLY WO/DRAINAGE BAG
K760253 · C.R. Bard, Inc. · Aug 1976