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FDA 510(k)

MOBILE MIM

K-Number: K103785 · 2011-02-04

ApplicantMim Software, Inc.
Decision Date2011-02-04
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOBILE MIM 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 2011-02-04 under 510(k) number K103785. 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 MOBILE MIM?

MOBILE MIM is a medical device that received FDA 510(k) clearance on 2011-02-04. The listed applicant is Mim Software, Inc.. The 510(k) number is K103785.

When did MOBILE MIM receive FDA 510(k) clearance?

MOBILE MIM received FDA 510(k) clearance on 2011-02-04, under 510(k) number K103785.

Who is the listed applicant for MOBILE MIM?

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 MOBILE MIM?

The FDA product code for MOBILE MIM is LLZ.

Related Clinical Trials

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.

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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

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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.

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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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