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FDA 510(k)

MEDICAL LE

K-Number: K020058 · 2002-04-04

ApplicantBarco N.V.
Decision Date2002-04-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDICAL LE is the device name listed in this FDA 510(k) record. The listed applicant is Barco N.V.. It received FDA 510(k) clearance on 2002-04-04 under 510(k) number K020058. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL LE?

MEDICAL LE is a medical device that received FDA 510(k) clearance on 2002-04-04. The listed applicant is Barco N.V.. The 510(k) number is K020058.

When did MEDICAL LE receive FDA 510(k) clearance?

MEDICAL LE received FDA 510(k) clearance on 2002-04-04, under 510(k) number K020058.

Who is the listed applicant for MEDICAL LE?

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

What is the FDA product code for MEDICAL LE?

The FDA product code for MEDICAL LE is LLZ.

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Related Devices (Code: LLZ)

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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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