FDA 510(k)

MicroTrend System

K-Number: K212425 · 2024-11-07

Decision Date2024-11-07

Product CodeCCK

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

MicroTrend System is a medical device manufactured by Exostat Medical, Inc.. It received FDA 510(k) clearance on 2024-11-07 under approval number K212425. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MicroTrend System?

MicroTrend System is a medical device that received FDA 510(k) clearance on 2024-11-07. It is manufactured by Exostat Medical, Inc.. The 510(k) number is K212425.

When was MicroTrend System approved by the FDA?

MicroTrend System received FDA 510(k) clearance on 2024-11-07, under approval number K212425.

What company makes MicroTrend System?

MicroTrend System is manufactured by Exostat Medical, Inc..

What is the FDA product code for MicroTrend System?

The FDA product code for MicroTrend System is CCK.

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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.