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FDA 510(k)

MAXCEM 2

K-Number: K073209 · 2008-01-29

ApplicantKerr Corporation
Decision Date2008-01-29
Product CodeMZW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MAXCEM 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 2008-01-29 under 510(k) number K073209. The device is classified under product code MZW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXCEM 2?

MAXCEM 2 is a medical device that received FDA 510(k) clearance on 2008-01-29. The listed applicant is Kerr Corporation. The 510(k) number is K073209.

When did MAXCEM 2 receive FDA 510(k) clearance?

MAXCEM 2 received FDA 510(k) clearance on 2008-01-29, under 510(k) number K073209.

Who is the listed applicant for MAXCEM 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 MAXCEM 2?

The FDA product code for MAXCEM 2 is MZW.

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Related Devices (Code: MZW)

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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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