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FDA 510(k)

ADMIRA SEAL

K-Number: K021842 · 2002-07-29

ApplicantVoco GmbH
Decision Date2002-07-29
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADMIRA 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 2002-07-29 under 510(k) number K021842. 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 ADMIRA SEAL?

ADMIRA SEAL is a medical device that received FDA 510(k) clearance on 2002-07-29. The listed applicant is Voco GmbH. The 510(k) number is K021842.

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

ADMIRA SEAL received FDA 510(k) clearance on 2002-07-29, under 510(k) number K021842.

Who is the listed applicant for ADMIRA 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 ADMIRA SEAL?

The FDA product code for ADMIRA SEAL is EBC.

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Other records listing Voco GmbH as applicant

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Related Devices (Code: EBC)

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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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