Cleared Traditional

K930135 - SILICONE RECTAL BALLOON

K930135 is the FDA 510(k) clearance for SILICONE RECTAL BALLOON by Cook Urological, Inc.. It is a Class 2 Gastroenterology & Urology device (product code FEN) cleared through the Traditional 510(k) pathway after a 269-day FDA review.

K930135 · Cook Urological, Inc. · Gastroenterology & Urology device
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Optimized for regulatory review, auditing and printing
Oct 1993
Decision
269d
Days
Class 2
Risk

K930135 is an FDA 510(k) clearance for the SILICONE RECTAL BALLOON. Classified as Device, Cystometric, Hydraulic (product code FEN), Class II - Special Controls.

Submitted by Cook Urological, Inc. (Spencer, US). The FDA issued a Cleared decision on October 8, 1993 after a review of 269 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1620 - 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

Submission Details

510(k) Number K930135 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 12, 1993
Decision Date October 08, 1993
Days to Decision 269 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
139d slower than avg
Panel avg: 130d · This submission: 269d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FEN Device, Cystometric, Hydraulic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1620
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 - FEN Device, Cystometric, Hydraulic

All 8
Devices cleared under the same product code (FEN) and FDA review panel - the closest regulatory comparables to K930135.
UROVISION JANUS
K953353 · Life-Tech Intl., Inc. · Sep 1995
TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS
K940203 · Life-Tech Intl., Inc. · Mar 1994
KENDALL URODYNAMIC CATHETERS
K933399 · Kendall Healthcare Products Co. Div.Of Tyco Health · Nov 1993
BARD URODYNAMIC CATHETER
K924714 · C.R. Bard, Inc. · Sep 1993