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FDA 510(k)

MIM-Ablation

K-Number: K220256 · 2022-10-07

ApplicantMim Software, Inc.
Decision Date2022-10-07
Product CodeQTZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM-Ablation is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2022-10-07 under approval number K220256. The device is classified under product code QTZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIM-Ablation?

MIM-Ablation is a medical device that received FDA 510(k) clearance on 2022-10-07. It is manufactured by Mim Software, Inc.. The 510(k) number is K220256.

When was MIM-Ablation approved by the FDA?

MIM-Ablation received FDA 510(k) clearance on 2022-10-07, under approval number K220256.

What company makes MIM-Ablation?

MIM-Ablation is manufactured by Mim Software, Inc..

What is the FDA product code for MIM-Ablation?

The FDA product code for MIM-Ablation is QTZ.

Other Devices by Mim Software, Inc.

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Related Devices (Code: QTZ)

K222222Artemis, Artemis TPO, Artemis MXEigen K222938Ablation-fitR.A.W. S.R.L K223639VisAble.IOTechsomed K240796myAblation Guide (VB80A)Siemens Healthcare GmbH K240773VisAble.IOTechsomed K251931BioTraceIO Vision (V1.7)Techsomed Medical Technologies

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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