Rusch International Urodynamic Catheters
FDA 510(k) K952029 · Rusch Intl.
510(k) numberK952029
Submission
- Device name
- Rusch International Urodynamic Catheters
- Applicant
- Rusch Intl.
Jeffrey, NH, US - Received
- May 1, 1995
- Decision date
- June 13, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FEN – Device, Cystometric, Hydraulic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1620
- Specialty
- Gastroenterology, Urology
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|---|---|---|---|
| K212830 | CT3000ProFEN · Traditional | Srs Medical | 12/21/2021SE |
| K082701 | Uronirs, Model 2000FEN · Traditional | Urodynamix Technologies, Ltd. | 12/18/2008SE |
| K073552 | Laborie Urodynamic System with Tetra AccessoryFEN · Traditional | Laborie Medical Technologies, Corp. | 03/05/2008SE |
| K001386 | Accuset Sensor, Model 2000FEN · Traditional | Pelvicare, Inc. | 07/17/2000SE |
| K992715 | Neuro Urodynamic Suite, Model 9032E0101FEN · Traditional | Medtronic Functional Diagnostics A/S | 02/28/2000SE |
| K983325 | In-Probe II Urodynamic SystemFEN · Traditional | Influence, Inc. | 11/24/1998SE |
| K970595 | Circon Endotek OM-4 H2O Cystometry PumpFEN · Traditional | Circon Video | 10/24/1997SE |
| K971911 | Lumax Cystometry Administration Tube SetFEN · Traditional | Medamicus, Inc. | 06/03/1997SE |
| K964522 | Ellipse 4FEN · Traditional | Andromeda Medizinische Systeme GmbH | 03/21/1997SE |
| K960503 | Dantec DuetFEN · Traditional | Dantec Medical, Inc. | 09/16/1996SE |
More from Dantec Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K033023 | Intermittent Urethral CathetersKOD · Traditional | 12/23/2003SE |
| K030559 | Rusch Polyflex Stent for the Esophagus W/Introducer/Delivery SystemESW · Traditional | 06/30/2003SE |
| K023666 | Rusch Guided Cholangiography CatheterFGE · Traditional | 06/17/2003SE |
| K023918 | Rusch Crystal Clear Tracheostomy Sets, Cuffed and CufflessJOH · Traditional | 03/28/2003SE |
| K023964 | Rusch Microlaryngeal TubeBTR · Traditional | 12/23/2002SE |
| K021540 | Rusch Edgar TubeBTR · Traditional | 08/01/2002SE |
| K021764 | Rusch Tracheofix Set, Cuffed and UncuffedBTO · Traditional | 07/23/2002SE |
| K020714 | Rusch Floneil; Flocath IntrogelGBM · Traditional | 07/01/2002SE |
| K010798 | Rusch Cantor TubeKNT · Traditional | 02/26/2002SE |
| K010797 | Rusch Miller-Abbott TubeKNT · Traditional | 02/26/2002SE |
Questions and answers
When was Rusch International Urodynamic Catheters cleared by the FDA?
Rusch International Urodynamic Catheters (K952029) received a 510(k) decision of Substantially Equivalent on June 13, 1995, 43 days after the submission was received.
What is the product code of K952029?
The FDA product code is FEN – Device, Cystometric, Hydraulic, a Class II (moderate risk) device regulated under 21 CFR 876.1620.