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FDA 510(k)

VITAL SIGNS MONITOR, MODEL: MD500B

K-Number: K082787 · 2009-01-12

ApplicantBeijing Choice Electronic Technololgy Co., Ltd.
Decision Date2009-01-12
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITAL SIGNS MONITOR, MODEL: MD500B 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 2009-01-12 under 510(k) number K082787. 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 VITAL SIGNS MONITOR, MODEL: MD500B?

VITAL SIGNS MONITOR, MODEL: MD500B is a medical device that received FDA 510(k) clearance on 2009-01-12. The listed applicant is Beijing Choice Electronic Technololgy Co., Ltd.. The 510(k) number is K082787.

When did VITAL SIGNS MONITOR, MODEL: MD500B receive FDA 510(k) clearance?

VITAL SIGNS MONITOR, MODEL: MD500B received FDA 510(k) clearance on 2009-01-12, under 510(k) number K082787.

Who is the listed applicant for VITAL SIGNS MONITOR, MODEL: MD500B?

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 VITAL SIGNS MONITOR, MODEL: MD500B?

The FDA product code for VITAL SIGNS MONITOR, MODEL: MD500B is MWI.

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

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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.

K260438Vital Signs Monitor (CLEO2)Infinium Medical, Inc.K253417Masimo Root Monitoring SystemMasimo CorporationK253196Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)Midmark CorporationK253436c-med0 alphaCosinuss GmbHK250135WAVE Clinical Platform (2.0.000)Baxter Healthcare Corp/ Excel MedicalK241766QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid)Fysicon BV

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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