Cleared Traditional

K901180 - FOLEY CATHETER INSERTION TRAY (30CC)

K901180 is an FDA 510(k) clearance for FOLEY CATHETER INSERTION TRAY (30CC), manufactured by Orion Life Systems, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FCM cleared through the Traditional 510(k) pathway after a 129-day FDA review.

K901180 · Orion Life Systems, Inc. · Gastroenterology & Urology device
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Jul 1990
Decision
129d
Days
Class 2
Risk

K901180 is an FDA 510(k) clearance for the FOLEY CATHETER INSERTION TRAY (30CC). Classified as Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) (product code FCM), Class II - Special Controls.

Submitted by Orion Life Systems, Inc. (Wheeling, US). The FDA issued a Cleared decision on July 20, 1990 after a review of 129 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 Orion Life Systems, Inc. devices

FDA 510(k) Submission Details - K901180

510(k) Number K901180 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received March 13, 1990
Decision Date July 20, 1990
Days to Decision 129 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
2d faster than avg
Panel avg: 131d · This submission: 129d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FCM Device Classification - Class 2, Special Controls

Product Code FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit)
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 - FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit)

All 31
Devices cleared under the same product code (FCM) and FDA review panel - the closest regulatory comparables to K901180.
FOLEY CATHETERIZATION TRAY
K942177 · Customed, Inc. · Sep 1994
MON-A-THERM FOLEY KIT
K923538 · Mallinckrodt Medical · May 1993
TOUCHLESS II INTERMITTENT CATHETER
K910653 · C.R. Bard, Inc. · May 1991
CATHETER CARE TRAY
K901181 · Orion Life Systems, Inc. · Jul 1990
URETHRAL CATHETER TRAY (PVC)
K901183 · Orion Life Systems, Inc. · Jul 1990
URETHRAL CATHETER TRAY (LATEX)
K901184 · Orion Life Systems, Inc. · Jul 1990