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FDA 510(k)

MIM – Y90 Dosimetry

K-Number: K172218 · 2017-11-21

Decision Date2017-11-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM – Y90 Dosimetry 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 2017-11-21 under 510(k) number K172218. 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 MIM – Y90 Dosimetry?

MIM – Y90 Dosimetry is a medical device that received FDA 510(k) clearance on 2017-11-21. The listed applicant is Mim Software, Inc.. The 510(k) number is K172218.

When did MIM – Y90 Dosimetry receive FDA 510(k) clearance?

MIM – Y90 Dosimetry received FDA 510(k) clearance on 2017-11-21, under 510(k) number K172218.

Who is the listed applicant for MIM – Y90 Dosimetry?

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 – Y90 Dosimetry?

The FDA product code for MIM – Y90 Dosimetry is LLZ.

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: 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.

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.