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FDA 510(k)

E-COM DR-2000 DR

K-Number: K193644 · 2020-02-14

ApplicantLivermoretech, Inc.
Decision Date2020-02-14
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

E-COM DR-2000 DR is the device name listed in this FDA 510(k) record. The listed applicant is Livermoretech, Inc.. It received FDA 510(k) clearance on 2020-02-14 under 510(k) number K193644. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-COM DR-2000 DR?

E-COM DR-2000 DR is a medical device that received FDA 510(k) clearance on 2020-02-14. The listed applicant is Livermoretech, Inc.. The 510(k) number is K193644.

When did E-COM DR-2000 DR receive FDA 510(k) clearance?

E-COM DR-2000 DR received FDA 510(k) clearance on 2020-02-14, under 510(k) number K193644.

Who is the listed applicant for E-COM DR-2000 DR?

The FDA 510(k) record lists Livermoretech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E-COM DR-2000 DR?

The FDA product code for E-COM DR-2000 DR is MQB.

Other records listing Livermoretech, Inc. 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.

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Related Devices (Code: MQB)

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.

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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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