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FDA 510(k)

METAMORPHOSIS

K-Number: K091023 · 2009-05-21

ApplicantKerr Corporation
Decision Date2009-05-21
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

METAMORPHOSIS is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2009-05-21 under 510(k) number K091023. 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 METAMORPHOSIS?

METAMORPHOSIS is a medical device that received FDA 510(k) clearance on 2009-05-21. The listed applicant is Kerr Corporation. The 510(k) number is K091023.

When did METAMORPHOSIS receive FDA 510(k) clearance?

METAMORPHOSIS received FDA 510(k) clearance on 2009-05-21, under 510(k) number K091023.

Who is the listed applicant for METAMORPHOSIS?

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 METAMORPHOSIS?

The FDA product code for METAMORPHOSIS is EBF.

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Related Devices (Code: 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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