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FDA 510(k)

MIM-Ablation

K-Number: K220256 · 2022-10-07

Decision Date2022-10-07
Product CodeQTZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM-Ablation 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 2022-10-07 under 510(k) 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. The listed applicant is Mim Software, Inc.. The 510(k) number is K220256.

When did MIM-Ablation receive FDA 510(k) clearance?

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

Who is the listed applicant for MIM-Ablation?

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-Ablation?

The FDA product code for MIM-Ablation is QTZ.

Other records listing Mim Software, 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.

View all 19 devices →

Related Devices (Code: QTZ)

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.

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.