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FDA 510(k)

CEMENTEK LV

K-Number: K042911 · 2004-12-27

ApplicantTeknimed, S.A.
Decision Date2004-12-27
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CEMENTEK LV is the device name listed in this FDA 510(k) record. The listed applicant is Teknimed, S.A.. It received FDA 510(k) clearance on 2004-12-27 under 510(k) number K042911. 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 CEMENTEK LV?

CEMENTEK LV is a medical device that received FDA 510(k) clearance on 2004-12-27. The listed applicant is Teknimed, S.A.. The 510(k) number is K042911.

When did CEMENTEK LV receive FDA 510(k) clearance?

CEMENTEK LV received FDA 510(k) clearance on 2004-12-27, under 510(k) number K042911.

Who is the listed applicant for CEMENTEK LV?

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

What is the FDA product code for CEMENTEK LV?

The FDA product code for CEMENTEK LV is MQV.

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Other records listing Teknimed, S.A. as applicant

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Related Devices (Code: MQV)

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

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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