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FDA 510(k)

REGISTRADO X-TRA

K-Number: K022066 · 2002-08-14

ApplicantVoco GmbH
Decision Date2002-08-14
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

REGISTRADO X-TRA is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2002-08-14 under 510(k) number K022066. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REGISTRADO X-TRA?

REGISTRADO X-TRA is a medical device that received FDA 510(k) clearance on 2002-08-14. The listed applicant is Voco GmbH. The 510(k) number is K022066.

When did REGISTRADO X-TRA receive FDA 510(k) clearance?

REGISTRADO X-TRA received FDA 510(k) clearance on 2002-08-14, under 510(k) number K022066.

Who is the listed applicant for REGISTRADO X-TRA?

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 REGISTRADO X-TRA?

The FDA product code for REGISTRADO X-TRA is ELW.

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Related Devices (Code: ELW)

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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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