Nova Balloon Thermodilution Infusion

FDA 510(k) K832287 · Nova Medical Specialties

Substantially Equivalent

510(k) numberK832287

Submission

Device name
Nova Balloon Thermodilution Infusion
Applicant
Nova Medical Specialties
Mchenry, IL, US
Received
July 13, 1983
Decision date
October 19, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DYG – Catheter, Flow Directed
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1240
Specialty
Cardiovascular

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K160084Swan Ganz CathetersDYG · Traditional Edwards Lifesciences, LLC05/03/2016SE
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More from Transonic Systems, Inc.

510(k)DeviceDecision
K872770Dual-Thermistor Thermodilution Cath. & Infu. Cath.DYG · Traditional 10/15/1987SE
K860526Nova Balloon Thermodilution Pressure Trans CathDXO · Traditional 05/02/1986SE
K853625Nova Arterial Embolectomy CatheterDXE · Traditional 01/15/1986SE
K840009Nova 12 Cardiac Output ComputerDXG · Traditional 08/22/1984SE
K841640Nova Balloon Thermodilution InfusionDYG · Traditional 08/12/1984SE
K841639Nova Balloon Thermodilution Cath.DYG · Traditional 08/12/1984SE
K834037Heparin Coated Balloon ThermodiluDYG · Traditional 01/10/1984SE
K834036Heparin Coated Balloon ThermodiluDYG · Traditional 01/10/1984SE
K822806Balloon Wedge Pressure, AngiographicDYG · Traditional 11/01/1982SE
K812761Flow-Directed Balloon ThermodilutionKRG · Traditional 11/02/1981SE

Questions and answers

When was Nova Balloon Thermodilution Infusion cleared by the FDA?

Nova Balloon Thermodilution Infusion (K832287) received a 510(k) decision of Substantially Equivalent on October 19, 1983, 98 days after the submission was received.

What is the product code of K832287?

The FDA product code is DYG – Catheter, Flow Directed, a Class II (moderate risk) device regulated under 21 CFR 870.1240.