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FDA 510(k)

MD2000A VITAL SIGN MONITOR, MODEL MD2000A

K-Number: K083466 · 2009-04-03

Decision Date2009-04-03
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MD2000A VITAL SIGN MONITOR, MODEL MD2000A 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 2009-04-03 under 510(k) number K083466. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD2000A VITAL SIGN MONITOR, MODEL MD2000A?

MD2000A VITAL SIGN MONITOR, MODEL MD2000A is a medical device that received FDA 510(k) clearance on 2009-04-03. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K083466.

When did MD2000A VITAL SIGN MONITOR, MODEL MD2000A receive FDA 510(k) clearance?

MD2000A VITAL SIGN MONITOR, MODEL MD2000A received FDA 510(k) clearance on 2009-04-03, under 510(k) number K083466.

Who is the listed applicant for MD2000A VITAL SIGN MONITOR, MODEL MD2000A?

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 MD2000A VITAL SIGN MONITOR, MODEL MD2000A?

The FDA product code for MD2000A VITAL SIGN MONITOR, MODEL MD2000A is DQA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Beijing Choice Electronic Technololgy Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 24 devices →

Related Devices (Code: DQA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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