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FDA 510(k)

BLOOD PRESSURE MONITOR, MODEL MD200A

K-Number: K093013 · 2010-01-08

ApplicantBeijing Choice Electronic Technololgy Co., Ltd.
Decision Date2010-01-08
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR, MODEL MD200A is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. It received FDA 510(k) clearance on 2010-01-08 under 510(k) number K093013. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD PRESSURE MONITOR, MODEL MD200A?

BLOOD PRESSURE MONITOR, MODEL MD200A is a medical device that received FDA 510(k) clearance on 2010-01-08. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K093013.

When did BLOOD PRESSURE MONITOR, MODEL MD200A receive FDA 510(k) clearance?

BLOOD PRESSURE MONITOR, MODEL MD200A received FDA 510(k) clearance on 2010-01-08, under 510(k) number K093013.

Who is the listed applicant for BLOOD PRESSURE MONITOR, MODEL MD200A?

The FDA 510(k) record lists Beijing Choice Electronic Technololgy Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MONITOR, MODEL MD200A?

The FDA product code for BLOOD PRESSURE MONITOR, MODEL MD200A is DXN.

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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.

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