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FDA 510(k)

CERUMEN FILTER

K-Number: K891594 · 1989-05-10

Decision Date1989-05-10
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CERUMEN FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Gn Danavox, Inc.. It received FDA 510(k) clearance on 1989-05-10 under 510(k) number K891594. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERUMEN FILTER?

CERUMEN FILTER is a medical device that received FDA 510(k) clearance on 1989-05-10. The listed applicant is Gn Danavox, Inc.. The 510(k) number is K891594.

When did CERUMEN FILTER receive FDA 510(k) clearance?

CERUMEN FILTER received FDA 510(k) clearance on 1989-05-10, under 510(k) number K891594.

Who is the listed applicant for CERUMEN FILTER?

The FDA 510(k) record lists Gn Danavox, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERUMEN FILTER?

The FDA product code for CERUMEN FILTER is ESD.

Related Clinical Trials

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.

Other records listing Gn Danavox, Inc. 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: ESD)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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