Cleared Traditional

K122785 - HYDROSIL

Also marketed or referenced as:
MAGIC PERSONAL CATHETER

K122785 is an FDA 510(k) clearance for HYDROSIL, manufactured by Rochester Medical Corp.. The device is a Class 2 Gastroenterology & Urology device with product code EZD cleared through the Traditional 510(k) pathway after a 245-day FDA review.

K122785 · Rochester Medical Corp. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2013
Decision
245d
Days
Class 2
Risk

K122785 is an FDA 510(k) clearance for the HYDROSIL. Classified as Catheter, Straight (product code EZD), Class II - Special Controls.

Submitted by Rochester Medical Corp. (Stewartville, US). The FDA issued a Cleared decision on May 14, 2013 after a review of 245 days - an extended review 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: 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 Rochester Medical Corp. devices

FDA 510(k) Submission Details - K122785

510(k) Number K122785 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 2012
Decision Date May 14, 2013
Days to Decision 245 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
114d slower than avg
Panel avg: 131d · This submission: 245d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EZD Device Classification - Class 2, Special Controls

Product Code EZD Catheter, Straight
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 - EZD Catheter, Straight

All 59
Devices cleared under the same product code (EZD) and FDA review panel - the closest regulatory comparables to K122785.
Well Lead PVC Urethral Catheter
K142563 · Well Lead Medical Co., Ltd. · Oct 2014
BARD RITECATH INTERMITTENT CATHETER
K133470 · C.R. Bard, Inc. · Apr 2014
WELL LEAD PVC HYDROPHILIC URETHRAL CATHETER
K133615 · Well Lead Medical Co., Ltd. · Feb 2014
LOFRIC PRIMO, LOFRIC HYDRO-KIT
K122078 · Astra Tech, Inc. · Oct 2012
COMFORTGLIDE INTERMITENT CATHETER
K112137 · C.R. Bard, Inc. · Aug 2011
CURE CATHETER
K110653 · Cure Medical, LLC · Aug 2011