Nova 12 Cardiac Output Computer
FDA 510(k) K840009 · Nova Medical Specialties
510(k) numberK840009
Submission
- Device name
- Nova 12 Cardiac Output Computer
- Applicant
- Nova Medical Specialties
Mchenry, IL, US - Received
- January 4, 1984
- Decision date
- August 22, 1984
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DXG – Computer, Diagnostic, Pre-Programmed, Single-Function
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1435
- Specialty
- Cardiovascular
Other 510(k)s with product code DXG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253092 | Argos Infinity (Rev. 1.0)DXG · Traditional | Retia Medical Systems, Inc. | 02/13/2026SE |
| K251275 | VitalStream ART Connect; VitalStream-HemoDXG · Traditional | Caretaker Medical | 09/26/2025SE |
| K232048 | Cogent Hemodynamic Monitoring System; Cogent HMSDXG · Traditional | Icu Medical | 12/20/2023SE |
| K212529 | Hypotension Decision Assist Model HDA-OR2DXG · Special | Directed Systems, Ltd. | 11/23/2021SE |
| K192169 | PulsioFlex Monitoring System with ProAQT SensorDXG · Traditional | Pulsion Medical Systems SE | 04/30/2020SE |
| K193179 | EV1000 Clinical PlatformDXG · Special | Edwards Lifesciences, LLC | 12/17/2019SE |
| K190955 | Hypotension Decision AssistDXG · Traditional | Directed Systems, Ltd. | 11/27/2019SE |
| K181372 | ArgosDXG · Traditional | Retia Medical, LLC | 12/13/2018SE |
| K172259 | PulsioFlex Monitoring SystemDXG · Traditional | Pulsion Medical Systems SE | 01/18/2018SE |
| K163334 | LiDCOunity v2 Hemodynamic MonitorDXG · Traditional | Lidco, Ltd. | 06/05/2017SE |
More from Lidco, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K872770 | Dual-Thermistor Thermodilution Cath. & Infu. Cath.DYG · Traditional | 10/15/1987SE |
| K860526 | Nova Balloon Thermodilution Pressure Trans CathDXO · Traditional | 05/02/1986SE |
| K853625 | Nova Arterial Embolectomy CatheterDXE · Traditional | 01/15/1986SE |
| K841640 | Nova Balloon Thermodilution InfusionDYG · Traditional | 08/12/1984SE |
| K841639 | Nova Balloon Thermodilution Cath.DYG · Traditional | 08/12/1984SE |
| K834037 | Heparin Coated Balloon ThermodiluDYG · Traditional | 01/10/1984SE |
| K834036 | Heparin Coated Balloon ThermodiluDYG · Traditional | 01/10/1984SE |
| K832287 | Nova Balloon Thermodilution InfusionDYG · Traditional | 10/19/1983SE |
| K822806 | Balloon Wedge Pressure, AngiographicDYG · Traditional | 11/01/1982SE |
| K812761 | Flow-Directed Balloon ThermodilutionKRG · Traditional | 11/02/1981SE |
Questions and answers
When was Nova 12 Cardiac Output Computer cleared by the FDA?
Nova 12 Cardiac Output Computer (K840009) received a 510(k) decision of Substantially Equivalent on August 22, 1984, 231 days after the submission was received.
What is the product code of K840009?
The FDA product code is DXG – Computer, Diagnostic, Pre-Programmed, Single-Function, a Class II (moderate risk) device regulated under 21 CFR 870.1435.