Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MIM - MRT Dosimetry

K-Number: K182624 · 2018-12-18

ApplicantMim Software, Inc.
Decision Date2018-12-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM - MRT 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 2018-12-18 under 510(k) number K182624. 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 - MRT Dosimetry?

MIM - MRT Dosimetry is a medical device that received FDA 510(k) clearance on 2018-12-18. The listed applicant is Mim Software, Inc.. The 510(k) number is K182624.

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

MIM - MRT Dosimetry received FDA 510(k) clearance on 2018-12-18, under 510(k) number K182624.

Who is the listed applicant for MIM - MRT 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 - MRT Dosimetry?

The FDA product code for MIM - MRT 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.

K253270Contour ProtégéAI+K251883MIM – LesionID ProK250035Contour ProtégéAI+K243012MIM – Symphony HDR FusionK233620MIM - Centiloid ScalingK232862MIM – Monte Carlo Dosimetry

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.

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

View on FDA Database →

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

↑