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FDA 510(k)

ECUSIT COMPOSITE REPAIR

K-Number: K992879 · 1999-11-09

ApplicantDmg Hamburg
Decision Date1999-11-09
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ECUSIT COMPOSITE REPAIR is the device name listed in this FDA 510(k) record. The listed applicant is Dmg Hamburg. It received FDA 510(k) clearance on 1999-11-09 under 510(k) number K992879. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECUSIT COMPOSITE REPAIR?

ECUSIT COMPOSITE REPAIR is a medical device that received FDA 510(k) clearance on 1999-11-09. The listed applicant is Dmg Hamburg. The 510(k) number is K992879.

When did ECUSIT COMPOSITE REPAIR receive FDA 510(k) clearance?

ECUSIT COMPOSITE REPAIR received FDA 510(k) clearance on 1999-11-09, under 510(k) number K992879.

Who is the listed applicant for ECUSIT COMPOSITE REPAIR?

The FDA 510(k) record lists Dmg Hamburg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECUSIT COMPOSITE REPAIR?

The FDA product code for ECUSIT COMPOSITE REPAIR is KLE.

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Related Devices (Code: KLE)

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

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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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