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FDA 510(k)

IONOLUX

K-Number: K090817 · 2009-07-23

ApplicantVoco GmbH
Decision Date2009-07-23
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IONOLUX is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2009-07-23 under 510(k) number K090817. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IONOLUX?

IONOLUX is a medical device that received FDA 510(k) clearance on 2009-07-23. The listed applicant is Voco GmbH. The 510(k) number is K090817.

When did IONOLUX receive FDA 510(k) clearance?

IONOLUX received FDA 510(k) clearance on 2009-07-23, under 510(k) number K090817.

Who is the listed applicant for IONOLUX?

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 IONOLUX?

The FDA product code for IONOLUX is EMA.

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Other records listing Voco GmbH as applicant

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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Related Devices (Code: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-PakK261166DIA-CEMDiaDent Group InternationalK254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, Inc.

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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