Breas Vivo Bilevel System, Model Vivo 40

FDA 510(k) K071702 · Breas Medical AB

Substantially Equivalent

510(k) numberK071702

Submission

Device name
Breas Vivo Bilevel System, Model Vivo 40
Applicant
Breas Medical AB
Molnlycke, SE
Received
June 21, 2007
Decision date
February 15, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MNT – Sv70 Ventilator
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5895
Specialty
Anesthesiology
Life-sustaining
Yes

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More from Respironics, Inc.

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K242485EveryWareMOD · Traditional 05/20/2025SE
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K240779Vivo 3MNT · Traditional 12/13/2024SE
K240778Vivo 1, Vivo 2MNS · Traditional 12/13/2024SE
K193586Vivo 45 LSNOU · Traditional 01/27/2021SE
K160481Vivo 60NOU · Traditional 11/09/2016SE
K090113Breas Vivo 40 SystemMNT · Traditional 05/14/2009SE
K063476Breas Isleep 20IBZD · Special 01/22/2007SE
K060657Isleep by Breas, Models Isleep 10, Isleep 20.BZD · Special 08/18/2006SE

Questions and answers

When was Breas Vivo Bilevel System, Model Vivo 40 cleared by the FDA?

Breas Vivo Bilevel System, Model Vivo 40 (K071702) received a 510(k) decision of Substantially Equivalent on February 15, 2008, 239 days after the submission was received.

What is the product code of K071702?

The FDA product code is MNT – Sv70 Ventilator, a Class II (moderate risk) device regulated under 21 CFR 868.5895.