Kendall Curity Suprapubic Catheter Tray, Kit, & Replacement Set
FDA 510(k) K970969 · The Kendal Co.
510(k) numberK970969
Submission
- Device name
- Kendall Curity Suprapubic Catheter Tray, Kit, & Replacement Set
- Applicant
- The Kendal Co.
Mansfield, MA, US - Received
- March 17, 1997
- Decision date
- April 23, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KOB – Catheter, Suprapubic (And Accessories)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5090
- Specialty
- Gastroenterology, Urology
- Implant
- Yes
Other 510(k)s with product code KOB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K240514 | AMT Low-Profile Suprapubic Catheter & Drainage SetKOB · Traditional | Applied Medical Technology, Inc. | 11/01/2024SE |
| K181097 | Cook Cystostomy Catheter SetKOB · Traditional | Cook Incorporated | 01/18/2019SESK |
| K182709 | One-Step Suprapubic IntroducerKOB · Traditional | Cook Incorporated | 12/26/2018SE |
| K182066 | O'Brien Suprapubic Introducer Set, Cook SP Tube Introducer SetKOB · Traditional | Cook Incorporated | 10/30/2018SESK |
| K132890 | Suprapubic Catheter and Introducer SetKOB · Traditional | Mediplus , Ltd. | 01/17/2014SE |
| K120127 | Swan Valley Medical Tranurethral Suprapubic Endo-Cystostomy (T-Spec) Surgical SystemKOB · Traditional | Swan Valley Medical, Incorporated | 10/26/2012SE |
| K014002 | All Silicone Supra-Pubia Catheter, Models 4880/4890KOB · Traditional | Fortune Medical Instrument Corp. | 03/04/2002SE |
| K012153 | Lowsley Suprapubic TractorKOB · Traditional | Circon Video | 09/19/2001SE |
| K970021 | Rusch Suprapubic TrayKOB · Traditional | Rusch, Inc. | 02/07/1997SE |
| K945480 | Moss(R) Steel Breakaway(R) IntroducerKOB · Traditional | Harry A. Schlakman | 08/28/1995SE |
More from Harry A. Schlakman
| 510(k) | Device | Decision |
|---|---|---|
| K000087 | Marhukar Triple Lumen Catheter, Model 12 FRFOZ · Traditional | 03/17/2000SE |
| K990500 | Kendall Ultramer Coude Foley Catheter, Model 1416C, Kendall Curity Coude Foley Catheter…EZL · Abbreviated | 09/28/1999SE |
| K991758 | Monoject Insulin SyringeFMF · Abbreviated | 06/14/1999SE |
| K951488 | Kendall Curity Catheter Plug with Protective CapKNY · Traditional | 04/25/1995SE |
| K942664 | Kendall Model 6325 SCD Sequel Compression SystemJOW · Traditional | 01/17/1995SE |
| K942774 | Polyskin(R) M.R. Moist Responsive Transparent DressingMGP · Traditional | 07/20/1994SN |
| K892434 | Kendall Curity Oxygen MaskBYG · Traditional | 08/15/1989SE |
| K892440 | Kendall Curity Extension TubesFPA · Traditional | 07/24/1989SE |
| K892438 | Kendall Curity Intravascular Cut Down TubesFPA · Traditional | 07/24/1989SE |
| K892436 | Kendall Curity Irrigation SyringeKOD · Traditional | 07/14/1989SE |
Questions and answers
When was Kendall Curity Suprapubic Catheter Tray, Kit, & Replacement Set cleared by the FDA?
Kendall Curity Suprapubic Catheter Tray, Kit, & Replacement Set (K970969) received a 510(k) decision of Substantially Equivalent on April 23, 1997, 37 days after the submission was received.
What is the product code of K970969?
The FDA product code is KOB – Catheter, Suprapubic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5090.