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FDA 510(k)

AiMIFY (1.x)

K-Number: K240290 · 2024-08-21

ApplicantSubtle Medical, Inc.
Decision Date2024-08-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AiMIFY (1.x) is the device name listed in this FDA 510(k) record. The listed applicant is Subtle Medical, Inc.. It received FDA 510(k) clearance on 2024-08-21 under 510(k) number K240290. 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 AiMIFY (1.x)?

AiMIFY (1.x) is a medical device that received FDA 510(k) clearance on 2024-08-21. The listed applicant is Subtle Medical, Inc.. The 510(k) number is K240290.

When did AiMIFY (1.x) receive FDA 510(k) clearance?

AiMIFY (1.x) received FDA 510(k) clearance on 2024-08-21, under 510(k) number K240290.

Who is the listed applicant for AiMIFY (1.x)?

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

What is the FDA product code for AiMIFY (1.x)?

The FDA product code for AiMIFY (1.x) is LLZ.

Other records listing Subtle Medical, Inc. 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.

K254120SubtleHD-CT (1.x)K254013SubtleHD-PET (1.x)K243250SubtleHD (1.x)K241329SubtleSYNTH (1.x)K233699SubtleREFORMAT (1.x)K223623SubtleMR (2.3.x)

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Related Devices (Code: LLZ)

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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLCK261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific CorporationK262143ImageGrid StreamVueCandelis, Inc.

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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