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FDA 510(k)

N-HYBRIDE-COMPOSITE LC

K-Number: K113563 · 2011-12-21

ApplicantVoco GmbH
Decision Date2011-12-21
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

N-HYBRIDE-COMPOSITE LC is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2011-12-21 under 510(k) number K113563. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N-HYBRIDE-COMPOSITE LC?

N-HYBRIDE-COMPOSITE LC is a medical device that received FDA 510(k) clearance on 2011-12-21. The listed applicant is Voco GmbH. The 510(k) number is K113563.

When did N-HYBRIDE-COMPOSITE LC receive FDA 510(k) clearance?

N-HYBRIDE-COMPOSITE LC received FDA 510(k) clearance on 2011-12-21, under 510(k) number K113563.

Who is the listed applicant for N-HYBRIDE-COMPOSITE LC?

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

What is the FDA product code for N-HYBRIDE-COMPOSITE LC?

The FDA product code for N-HYBRIDE-COMPOSITE LC is EBF.

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Other records listing Voco GmbH as applicant

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Related Devices (Code: EBF)

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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