FDA 510(k)

BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5

K-Number: K092449 · 2010-08-30

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd.

Decision Date2010-08-30

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2010-08-30 under 510(k) number K092449. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5?

BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5 is a medical device that received FDA 510(k) clearance on 2010-08-30. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K092449.

When did BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5 receive FDA 510(k) clearance?

BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5 received FDA 510(k) clearance on 2010-08-30, under 510(k) number K092449.

Who is the listed applicant for BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5?

The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5?

The FDA product code for BENEVIEW T SERIES PATIENT MONITORS, MODELS BENEVIEW T8, T6 AND T5 is MHX.

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Official Source

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