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FDA 510(k)

MYLABFIVE

K-Number: K083882 · 2009-01-30

Decision Date2009-01-30
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MYLABFIVE is the device name listed in this FDA 510(k) record. The listed applicant is Esaote Europe B.V.. It received FDA 510(k) clearance on 2009-01-30 under 510(k) number K083882. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYLABFIVE?

MYLABFIVE is a medical device that received FDA 510(k) clearance on 2009-01-30. The listed applicant is Esaote Europe B.V.. The 510(k) number is K083882.

When did MYLABFIVE receive FDA 510(k) clearance?

MYLABFIVE received FDA 510(k) clearance on 2009-01-30, under 510(k) number K083882.

Who is the listed applicant for MYLABFIVE?

The FDA 510(k) record lists Esaote Europe B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYLABFIVE?

The FDA product code for MYLABFIVE is IYN.

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 Esaote Europe B.V. 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.

Related Devices (Code: IYN)

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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