Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes

FDA 510(k) K221782 · Merit Medical Pte. , Ltd.

Substantially Equivalent

510(k) numberK221782

Submission

Device name
Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes
Applicant
Merit Medical Pte. , Ltd.
Singapore, SG
Received
June 21, 2022
Decision date
March 17, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DRS – Transducer, Blood-Pressure, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2850
Specialty
Cardiovascular

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K161408Compass Cast and MAPDRS · Traditional Centurion Medical Products Corporation11/22/2016SE
K152472Disposable Pressure TransducerDRS · Traditional Zhejiang Haisheng Medical Device Co., Ltd.10/31/2016SE
K152980Flo Trac sensor, Volume View sensorDRS · Traditional Edwards Lifesciences, LLC01/19/2016SE
K151040Art-line Single channel blood pressure system, Art-line Double channel blood pressure…DRS · Traditional Biometrix , Ltd.09/04/2015SE
K133624Compass CT, Compass CT PortDRS · Traditional Mirador Biomedical04/18/2014SE
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Questions and answers

When was Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes cleared by the FDA?

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes (K221782) received a 510(k) decision of Substantially Equivalent on March 17, 2023, 269 days after the submission was received.

What is the product code of K221782?

The FDA product code is DRS – Transducer, Blood-Pressure, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2850.