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FDA 510(k)

GRANDIO SEAL

K-Number: K062344 · 2006-10-02

ApplicantVoco GmbH
Decision Date2006-10-02
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GRANDIO SEAL is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2006-10-02 under 510(k) number K062344. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRANDIO SEAL?

GRANDIO SEAL is a medical device that received FDA 510(k) clearance on 2006-10-02. The listed applicant is Voco GmbH. The 510(k) number is K062344.

When did GRANDIO SEAL receive FDA 510(k) clearance?

GRANDIO SEAL received FDA 510(k) clearance on 2006-10-02, under 510(k) number K062344.

Who is the listed applicant for GRANDIO SEAL?

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 GRANDIO SEAL?

The FDA product code for GRANDIO SEAL is EBC.

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Other records listing Voco GmbH as applicant

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Related Devices (Code: EBC)

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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