Wedge Pressure Catheter Flow Directed
FDA 510(k) K841705 · Mansfield Scientific, Inc.
510(k) numberK841705
Submission
- Device name
- Wedge Pressure Catheter Flow Directed
- Applicant
- Mansfield Scientific, Inc.
Walker, MI, US - Received
- April 23, 1984
- Decision date
- July 13, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DYG – Catheter, Flow Directed
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1240
- Specialty
- Cardiovascular
Other 510(k)s with product code DYG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K242451 | HemoSphere Alta Advanced Monitoring Platform (ALTAALL1/ALTCR1/ALTASR1); HemoSphere Alta-…DYG · Traditional | Edwards Lifesciences | 12/09/2024SE |
| K233983 | Swan-Ganz Pacing Probe and Catheters; Swan-Ganz Bipolar Pacing Catheter (D97120F5)…DYG · Traditional | Edwards Lifesciences | 06/27/2024SE |
| K233824 | Swan-Ganz catheterDYG · Traditional | Edwards Lifesciences, LLC | 06/06/2024SE |
| K231248 | Swan-Ganz Catheters, FloTrac sensors, ClearSight finger cuffs, HemoSphere Advanced…DYG · Traditional | Edwards Lifesciencess, LLC | 09/21/2023SE |
| K222117 | Swang-Ganz IQ pulmonary artery catheterDYG · Traditional | Edwards Lifesiences, LLC | 12/09/2022SE |
| K193466 | Swan-Ganz CathetersDYG · Traditional | Edwards Lifesciences, LLC | 02/16/2020SE |
| K160084 | Swan Ganz CathetersDYG · Traditional | Edwards Lifesciences, LLC | 05/03/2016SE |
| K094048 | Percupro Messenger Balloon CatheterDYG · Traditional | Cardiosolutions, Inc. | 07/14/2011SE |
| K081052 | Occlusion Balloon Catheter, Model VenosDYG · Traditional | Oscor, Inc. | 06/18/2008SE |
| K010253 | Angio Flow Thermodilution Catheter, Model AF-CATH-01; Angioflow Meter, Models HQ100 and…DYG · Traditional | Transonic Systems, Inc. | 03/19/2002SE |
More from Transonic Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K865017 | AngioscopeDQX · Traditional | 12/15/1987SE |
| K870186 | Endomyocardial Biopsy DeviceDWZ · Traditional | 02/20/1987SE |
| K855103 | Ciribart Gyudubg CatgeterDQO · Traditional | 02/18/1986SE |
| K853850 | ExplorerDTB · Traditional | 12/04/1985SE |
| K852797 | Heparin Coat Tran Ballo Tip Temp Pac ElectrodeLDF · Traditional | 09/16/1985SE |
| K851848 | Percutaneous Transluminal Blood Dilation CatheterLIT · Traditional | 07/19/1985SE |
| K844752 | Transvenous Balloon Tipped(Flow Directed) Temp. PaDTB · Traditional | 01/02/1985SE |
Questions and answers
When was Wedge Pressure Catheter Flow Directed cleared by the FDA?
Wedge Pressure Catheter Flow Directed (K841705) received a 510(k) decision of Substantially Equivalent on July 13, 1984, 81 days after the submission was received.
What is the product code of K841705?
The FDA product code is DYG – Catheter, Flow Directed, a Class II (moderate risk) device regulated under 21 CFR 870.1240.