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FDA 510(k)

MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE

K-Number: K051528 · 2005-07-20

ApplicantMevis Technology GmbH & Co. KG
Decision Date2005-07-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Mevis Technology GmbH & Co. KG. It received FDA 510(k) clearance on 2005-07-20 under 510(k) number K051528. 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 MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE?

MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE is a medical device that received FDA 510(k) clearance on 2005-07-20. The listed applicant is Mevis Technology GmbH & Co. KG. The 510(k) number is K051528.

When did MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE receive FDA 510(k) clearance?

MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE received FDA 510(k) clearance on 2005-07-20, under 510(k) number K051528.

Who is the listed applicant for MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE?

The FDA 510(k) record lists Mevis Technology GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE?

The FDA product code for MEVIS LIVERANALYSER/LIVERVIEWER SOFTWARE is 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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