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

FDA 510(k)

MD2000B VITAL SIGN MONITOR, MODEL MD2000B

K-Number: K100740 · 2010-07-09

Decision Date2010-07-09
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MD2000B VITAL SIGN MONITOR, MODEL MD2000B 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 2010-07-09 under 510(k) number K100740. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD2000B VITAL SIGN MONITOR, MODEL MD2000B?

MD2000B VITAL SIGN MONITOR, MODEL MD2000B is a medical device that received FDA 510(k) clearance on 2010-07-09. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K100740.

When did MD2000B VITAL SIGN MONITOR, MODEL MD2000B receive FDA 510(k) clearance?

MD2000B VITAL SIGN MONITOR, MODEL MD2000B received FDA 510(k) clearance on 2010-07-09, under 510(k) number K100740.

Who is the listed applicant for MD2000B VITAL SIGN MONITOR, MODEL MD2000B?

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 MD2000B VITAL SIGN MONITOR, MODEL MD2000B?

The FDA product code for MD2000B VITAL SIGN MONITOR, MODEL MD2000B is MWI.

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: MWI)

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

View on FDA Database →

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

↑