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FDA 510(k)

MTA2.2 MATERIAL

K-Number: K161239 · 2016-09-01

ApplicantAvalon Biomed, Inc.
Decision Date2016-09-01
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MTA2.2 MATERIAL is a medical device manufactured by Avalon Biomed, Inc.. It received FDA 510(k) clearance on 2016-09-01 under approval number K161239. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTA2.2 MATERIAL?

MTA2.2 MATERIAL is a medical device that received FDA 510(k) clearance on 2016-09-01. It is manufactured by Avalon Biomed, Inc.. The 510(k) number is K161239.

When was MTA2.2 MATERIAL approved by the FDA?

MTA2.2 MATERIAL received FDA 510(k) clearance on 2016-09-01, under approval number K161239.

What company makes MTA2.2 MATERIAL?

MTA2.2 MATERIAL is manufactured by Avalon Biomed, Inc..

What is the FDA product code for MTA2.2 MATERIAL?

The FDA product code for MTA2.2 MATERIAL is KIF.

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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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