FDA 510(k)

IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS

K-Number: K123074 · 2013-07-03

ApplicantShenzhen Mindray Bio-Medical Electronics Co., Ltd.

Decision Date2013-07-03

Product CodeMHX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS 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 2013-07-03 under 510(k) number K123074. 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 IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS?

IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS is a medical device that received FDA 510(k) clearance on 2013-07-03. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K123074.

When did IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS receive FDA 510(k) clearance?

IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS received FDA 510(k) clearance on 2013-07-03, under 510(k) number K123074.

Who is the listed applicant for IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS?

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 IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS?

The FDA product code for IMEC, IPM AND BENEVIEW T1 PATIENT MONITORS is MHX.

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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.