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FDA 510(k)

GENEROS 80, GENEROS 60

K-Number: K051914 · 2005-11-03

ApplicantBerkeley Advanced Biomaterials, Inc.
Decision Date2005-11-03
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

GENEROS 80, GENEROS 60 is the device name listed in this FDA 510(k) record. The listed applicant is Berkeley Advanced Biomaterials, Inc.. It received FDA 510(k) clearance on 2005-11-03 under 510(k) number K051914. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENEROS 80, GENEROS 60?

GENEROS 80, GENEROS 60 is a medical device that received FDA 510(k) clearance on 2005-11-03. The listed applicant is Berkeley Advanced Biomaterials, Inc.. The 510(k) number is K051914.

When did GENEROS 80, GENEROS 60 receive FDA 510(k) clearance?

GENEROS 80, GENEROS 60 received FDA 510(k) clearance on 2005-11-03, under 510(k) number K051914.

Who is the listed applicant for GENEROS 80, GENEROS 60?

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

What is the FDA product code for GENEROS 80, GENEROS 60?

The FDA product code for GENEROS 80, GENEROS 60 is MQV.

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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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