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FDA 510(k)

VINT

K-Number: K240385 · 2024-10-15

ApplicantMediimg Corporation
Decision Date2024-10-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VINT is the device name listed in this FDA 510(k) record. The listed applicant is Mediimg Corporation. It received FDA 510(k) clearance on 2024-10-15 under 510(k) number K240385. 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 VINT?

VINT is a medical device that received FDA 510(k) clearance on 2024-10-15. The listed applicant is Mediimg Corporation. The 510(k) number is K240385.

When did VINT receive FDA 510(k) clearance?

VINT received FDA 510(k) clearance on 2024-10-15, under 510(k) number K240385.

Who is the listed applicant for VINT?

The FDA 510(k) record lists Mediimg Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINT?

The FDA product code for VINT is LLZ.

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

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

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