Cleared Traditional

K910876 - AUTOCATH(TM) SET

K910876 is the FDA 510(k) clearance for AUTOCATH(TM) SET by Cook Urological, Inc.. It is a Class 2 Gastroenterology & Urology device (product code GBM) cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K910876 · Cook Urological, Inc. · Gastroenterology & Urology device
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May 1991
Decision
88d
Days
Class 2
Risk

K910876 is an FDA 510(k) clearance for the AUTOCATH(TM) SET. Classified as Catheter, Urethral (product code GBM), Class II - Special Controls.

Submitted by Cook Urological, Inc. (Spencer, US). The FDA issued a Cleared decision on May 28, 1991 after a review of 88 days - a notably fast clearance cycle.

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: 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 Cook Urological, Inc. devices

Submission Details

510(k) Number K910876 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 01, 1991
Decision Date May 28, 1991
Days to Decision 88 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 130d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 40
Devices cleared under the same product code (GBM) and FDA review panel - the closest regulatory comparables to K910876.
SPEEDICATH
K023254 · Coloplast Corp. · Jan 2003
DILATION CATHETER, BALLOON
K965067 · Boston Scientific Corp · Jan 1997
ENTRAC(TM) URETHRAL MEASURING CATHETER
K914905 · American Medical Systems, Inc. · Mar 1992
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