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FDA 510(k)

DMC COMPOSITE 2

K-Number: K103351 · 2011-01-20

ApplicantKerr Corporation
Decision Date2011-01-20
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DMC COMPOSITE 2 is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2011-01-20 under 510(k) number K103351. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMC COMPOSITE 2?

DMC COMPOSITE 2 is a medical device that received FDA 510(k) clearance on 2011-01-20. The listed applicant is Kerr Corporation. The 510(k) number is K103351.

When did DMC COMPOSITE 2 receive FDA 510(k) clearance?

DMC COMPOSITE 2 received FDA 510(k) clearance on 2011-01-20, under 510(k) number K103351.

Who is the listed applicant for DMC COMPOSITE 2?

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

What is the FDA product code for DMC COMPOSITE 2?

The FDA product code for DMC COMPOSITE 2 is EBF.

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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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