Uni-Vent (R) Model 731 Series Portable Critical Care Ventilator

FDA 510(k) K111473 · Impact Instrumentation, Inc.

Substantially Equivalent

510(k) numberK111473

Submission

Device name
Uni-Vent (R) Model 731 Series Portable Critical Care Ventilator
Applicant
Impact Instrumentation, Inc.
West Caldwell, NJ, US
Received
May 27, 2011
Decision date
February 16, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CBK – Ventilator, Continuous, Facility Use
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5895
Specialty
Anesthesiology
Life-sustaining
Yes

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More from Flight Medical Innovations , Ltd.

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K071526Uni-Vent 731 Series Ventilators, Model 731, 731EMVCBK · Traditional 12/10/2008SE
K051476Uni-Vent Model 73XBTL · Traditional 10/28/2005SE
K032386Uni-Vent Model 730AEV (Automatic Emergency Ventilator)BTL · Traditional 03/26/2004SE
K022062Impact, Universal Single-Limb, Ventilator Circuit, Model 820-0099-00MOD · Abbreviated 05/06/2003SE
K951423Aspirator, Continuous & Programmable IntermittentBTA · Traditional 04/18/1995SE
K941096Electric Vacum PumpBTA · Traditional 01/05/1995SE
K931473Impact Model 753BTL · Traditional 12/30/1994SE

Questions and answers

When was Uni-Vent (R) Model 731 Series Portable Critical Care Ventilator cleared by the FDA?

Uni-Vent (R) Model 731 Series Portable Critical Care Ventilator (K111473) received a 510(k) decision of Substantially Equivalent on February 16, 2012, 265 days after the submission was received.

What is the product code of K111473?

The FDA product code is CBK – Ventilator, Continuous, Facility Use, a Class II (moderate risk) device regulated under 21 CFR 868.5895.