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FDA 510(k)

Linshom Respiratory Monitoring Device (LRMD)

K-Number: K190734 · 2020-01-30

ApplicantLinshom Management, LLC
Decision Date2020-01-30
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Linshom Respiratory Monitoring Device (LRMD) is a medical device manufactured by Linshom Management, LLC. It received FDA 510(k) clearance on 2020-01-30 under approval number K190734. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Linshom Respiratory Monitoring Device (LRMD)?

Linshom Respiratory Monitoring Device (LRMD) is a medical device that received FDA 510(k) clearance on 2020-01-30. It is manufactured by Linshom Management, LLC. The 510(k) number is K190734.

When was Linshom Respiratory Monitoring Device (LRMD) approved by the FDA?

Linshom Respiratory Monitoring Device (LRMD) received FDA 510(k) clearance on 2020-01-30, under approval number K190734.

What company makes Linshom Respiratory Monitoring Device (LRMD)?

Linshom Respiratory Monitoring Device (LRMD) is manufactured by Linshom Management, LLC.

What is the FDA product code for Linshom Respiratory Monitoring Device (LRMD)?

The FDA product code for Linshom Respiratory Monitoring Device (LRMD) is BZQ.

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Related PubMed Literature

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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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