Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes

K-Number: K221782 · 2023-03-17

Decision Date2023-03-17
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is a medical device manufactured by Merit Medical Pte. , Ltd.. It received FDA 510(k) clearance on 2023-03-17 under approval number K221782. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes?

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is a medical device that received FDA 510(k) clearance on 2023-03-17. It is manufactured by Merit Medical Pte. , Ltd.. The 510(k) number is K221782.

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

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes received FDA 510(k) clearance on 2023-03-17, under approval number K221782.

What company makes Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes?

Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is manufactured by Merit Medical Pte. , Ltd..

What is the FDA product code for Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes?

The FDA product code for Meritrans ECO Reusable Pressure Transducer, Meritrans ECO Domes is DRS.

Related Devices (Code: DRS)

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.