Rusch Simplastic Foley Catheterization Set

FDA 510(k) K963993 · Rusch, Inc.

Substantially Equivalent

510(k) numberK963993

Submission

Device name
Rusch Simplastic Foley Catheterization Set
Applicant
Rusch, Inc.
Jeffrey, NH, US
Received
October 4, 1996
Decision date
December 17, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FCM – Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

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K030712Amsure Urethral Catheterization TrayFCM · Traditional Amsino International, Inc.05/23/2003SE
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K011055The O'Neil Sterile Field Urinary Catheter Kit with Prep PadsFCM · Traditional Go Medical Industries Pty. , Ltd.06/06/2001SE
K010420Rusch Mmg/O'Neil CatheterFCM · Traditional Rusch, Inc.05/09/2001SE

More from Rusch, Inc.

510(k)DeviceDecision
K010420Rusch Mmg/O'Neil CatheterFCM · Traditional 05/09/2001SE
K993528Rusch Emergency MaskCBP · Traditional 05/31/2000SE
K993194Rusch Manual Resuscitator BagBTM · Traditional 03/24/2000SE
K980870Rusch Silicone Foley CatheterEZL · Traditional 06/09/1998SE
K974419Rusch Simplastic Councill Tip CatheterEZL · Traditional 01/27/1998SE
K963779Rusch Enteral Feeding TubeFPD · Traditional 05/23/1997SE
K970021Rusch Suprapubic TrayKOB · Traditional 02/07/1997SE
K955564Rusch Ultra Tracheoflex Tracheostomy Set, Cuffed, SterileJOH · Traditional 06/28/1996SE
K955495Rusch Reinforced Trachael Tube Cuffed, SterileBTR · Traditional 06/27/1996SE
K953963Rusch Single Lumen Bronchial Tuvbe Set, Sterile, for Left & Right Sided Bronchial…BTS · Traditional 11/27/1995SE

Questions and answers

When was Rusch Simplastic Foley Catheterization Set cleared by the FDA?

Rusch Simplastic Foley Catheterization Set (K963993) received a 510(k) decision of Substantially Equivalent on December 17, 1996, 74 days after the submission was received.

What is the product code of K963993?

The FDA product code is FCM – Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit), a Class II (moderate risk) device regulated under 21 CFR 876.5130.