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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 the device name listed in this FDA 510(k) record. The listed applicant is Mim Software, Inc.. It received FDA 510(k) clearance on 2024-10-23 under 510(k) 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. The listed applicant is Mim Software, Inc.. The 510(k) number is K243012.

When did MIM – Symphony HDR Fusion receive FDA 510(k) clearance?

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

Who is the listed applicant for MIM – Symphony HDR Fusion?

The FDA 510(k) record lists Mim Software, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Mim Software, Inc. as applicant

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Related Devices (Code: 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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