MIM-Ablation
K-Number: K220256 · 2022-10-07
Device Summary
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.
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.