Puritan Bennett Cuff Pressure Manager
K-Number: K202874 · 2021-01-09
ApplicantCovidien, LLC
Decision Date2021-01-09
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Puritan Bennett Cuff Pressure Manager is a medical device manufactured by Covidien, LLC. It received FDA 510(k) clearance on 2021-01-09 under approval number K202874. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Puritan Bennett Cuff Pressure Manager?
Puritan Bennett Cuff Pressure Manager is a medical device that received FDA 510(k) clearance on 2021-01-09. It is manufactured by Covidien, LLC. The 510(k) number is K202874.
When was Puritan Bennett Cuff Pressure Manager approved by the FDA?
Puritan Bennett Cuff Pressure Manager received FDA 510(k) clearance on 2021-01-09, under approval number K202874.
What company makes Puritan Bennett Cuff Pressure Manager?
Puritan Bennett Cuff Pressure Manager is manufactured by Covidien, LLC.
What is the FDA product code for Puritan Bennett Cuff Pressure Manager?
The FDA product code for Puritan Bennett Cuff Pressure Manager is BSK.
Other Devices by Covidien, LLC
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K180991AG 100sHospitech Respiration , Ltd.
K173914VORTRAN Cuff Inflator (VCI)Vortran Medical Technology 1, Inc.
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.