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FDA 510(k)

Y-MIC

K-Number: K161639 · 2016-12-22

Decision Date2016-12-22
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Y-MIC is the device name listed in this FDA 510(k) record. The listed applicant is Micron Corporation. It received FDA 510(k) clearance on 2016-12-22 under 510(k) number K161639. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Y-MIC?

Y-MIC is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Micron Corporation. The 510(k) number is K161639.

When did Y-MIC receive FDA 510(k) clearance?

Y-MIC received FDA 510(k) clearance on 2016-12-22, under 510(k) number K161639.

Who is the listed applicant for Y-MIC?

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

What is the FDA product code for Y-MIC?

The FDA product code for Y-MIC is ELC.

Other records listing Micron Corporation as applicant

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.

Related Devices (Code: ELC)

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.

Official Source

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