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FDA 510(k)

MICSI-RMT

K-Number: K241121 · 2024-07-17

ApplicantMicrostructure Imaging, Inc.
Decision Date2024-07-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICSI-RMT is a medical device manufactured by Microstructure Imaging, Inc.. It received FDA 510(k) clearance on 2024-07-17 under approval number K241121. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICSI-RMT?

MICSI-RMT is a medical device that received FDA 510(k) clearance on 2024-07-17. It is manufactured by Microstructure Imaging, Inc.. The 510(k) number is K241121.

When was MICSI-RMT approved by the FDA?

MICSI-RMT received FDA 510(k) clearance on 2024-07-17, under approval number K241121.

What company makes MICSI-RMT?

MICSI-RMT is manufactured by Microstructure Imaging, Inc..

What is the FDA product code for MICSI-RMT?

The FDA product code for MICSI-RMT is LLZ.

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Official Source

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