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FDA 510(k)

MIM – Symphony HDR Fusion

K-Number: K243012 · 2024-10-23

ApplicantMim Software, Inc.
Decision Date2024-10-23
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM – Symphony HDR Fusion is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2024-10-23 under approval number K243012. 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 MIM – Symphony HDR Fusion?

MIM – Symphony HDR Fusion is a medical device that received FDA 510(k) clearance on 2024-10-23. It is manufactured by Mim Software, Inc.. The 510(k) number is K243012.

When was MIM – Symphony HDR Fusion approved by the FDA?

MIM – Symphony HDR Fusion received FDA 510(k) clearance on 2024-10-23, under approval number K243012.

What company makes MIM – Symphony HDR Fusion?

MIM – Symphony HDR Fusion is manufactured by Mim Software, Inc..

What is the FDA product code for MIM – Symphony HDR Fusion?

The FDA product code for MIM – Symphony HDR Fusion is LLZ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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