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FDA 510(k)

MESODERM

K-Number: K061849 · 2007-04-30

ApplicantAa Advanced Technology, Inc.
Decision Date2007-04-30
Product CodeEGJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MESODERM is the device name listed in this FDA 510(k) record. The listed applicant is Aa Advanced Technology, Inc.. It received FDA 510(k) clearance on 2007-04-30 under 510(k) number K061849. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MESODERM?

MESODERM is a medical device that received FDA 510(k) clearance on 2007-04-30. The listed applicant is Aa Advanced Technology, Inc.. The 510(k) number is K061849.

When did MESODERM receive FDA 510(k) clearance?

MESODERM received FDA 510(k) clearance on 2007-04-30, under 510(k) number K061849.

Who is the listed applicant for MESODERM?

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

What is the FDA product code for MESODERM?

The FDA product code for MESODERM is EGJ.

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Related Devices (Code: EGJ)

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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