Cleared Traditional

K896160 - WILLIAMS PENILE ANESTHETIC RETAINER

K896160 is an FDA 510(k) clearance for WILLIAMS PENILE ANESTHETIC RETAINER, manufactured by Cook Urological, Inc.. The device is a Class 1 Gastroenterology & Urology device with product code FHA cleared through the Traditional 510(k) pathway after a 115-day FDA review.

K896160 · Cook Urological, Inc. · Gastroenterology & Urology device
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Optimized for regulatory review, auditing and printing
Feb 1990
Decision
115d
Days
Class 1
Risk

K896160 is an FDA 510(k) clearance for the WILLIAMS PENILE ANESTHETIC RETAINER. Classified as Clamp, Penile (product code FHA), Class I - General Controls.

Submitted by Cook Urological, Inc. (Spencer, US). The FDA issued a Cleared decision on February 16, 1990 after a review of 115 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5160 - 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 Cook Urological, Inc. devices

FDA 510(k) Submission Details - K896160

510(k) Number K896160 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 24, 1989
Decision Date February 16, 1990
Days to Decision 115 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
16d faster than avg
Panel avg: 131d · This submission: 115d
Pathway characteristics
Predicate-based equivalence.

FHA Device Classification - Class 1, General Controls

Product Code FHA Clamp, Penile
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.5160
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FHA Clamp, Penile

All 7
Devices cleared under the same product code (FHA) and FDA review panel - the closest regulatory comparables to K896160.
MENTOR UROLOGY TRIPLE RIB OCCLUSION WRAP FOR MALE INCONTINENCE
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U-TEX
K955810 · Laborie Medical Technologies, Ltd. · Jan 1996
DACOMED EXTERNAL MALE CONTINENCE DEVICE
K885323 · Dacomed Corp. · Feb 1989
COOK-VPI CONTINENCE CUFF
K863227 · Cook Urological, Inc. · Feb 1987