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FDA 510(k)

Puritan Bennett 840 Series Ventilator System

K-Number: K151252 · 2016-03-29

ApplicantCovidien LP
Decision Date2016-03-29
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Puritan Bennett 840 Series Ventilator System is a medical device manufactured by Covidien LP. It received FDA 510(k) clearance on 2016-03-29 under approval number K151252. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Puritan Bennett 840 Series Ventilator System?

Puritan Bennett 840 Series Ventilator System is a medical device that received FDA 510(k) clearance on 2016-03-29. It is manufactured by Covidien LP. The 510(k) number is K151252.

When was Puritan Bennett 840 Series Ventilator System approved by the FDA?

Puritan Bennett 840 Series Ventilator System received FDA 510(k) clearance on 2016-03-29, under approval number K151252.

What company makes Puritan Bennett 840 Series Ventilator System?

Puritan Bennett 840 Series Ventilator System is manufactured by Covidien LP.

What is the FDA product code for Puritan Bennett 840 Series Ventilator System?

The FDA product code for Puritan Bennett 840 Series Ventilator System is CBK.

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Related PubMed Literature

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Related Devices (Code: CBK)

K153046HAMILTON-MR1Hamilton Medical AG K152068Astral 100/150Resmed, Ltd. K143035Flight 60 VentilatorFlight Medical Innovations , Ltd. K162738Puritan Bennett 980 Ventilator SystemCovidien K170037Breathe Technologies Life2000™ Ventilation SystemBreathe Technologies K162832731 Series VentilatorsZOLL Medical Corporation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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