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FDA 510(k)

MIPLATFORM MEDICAL IMAGING SUITE

K-Number: K131424 · 2013-07-12

ApplicantHinacom Software and Technology, Ltd.
Decision Date2013-07-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIPLATFORM MEDICAL IMAGING SUITE is the device name listed in this FDA 510(k) record. The listed applicant is Hinacom Software and Technology, Ltd.. It received FDA 510(k) clearance on 2013-07-12 under 510(k) number K131424. 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 MIPLATFORM MEDICAL IMAGING SUITE?

MIPLATFORM MEDICAL IMAGING SUITE is a medical device that received FDA 510(k) clearance on 2013-07-12. The listed applicant is Hinacom Software and Technology, Ltd.. The 510(k) number is K131424.

When did MIPLATFORM MEDICAL IMAGING SUITE receive FDA 510(k) clearance?

MIPLATFORM MEDICAL IMAGING SUITE received FDA 510(k) clearance on 2013-07-12, under 510(k) number K131424.

Who is the listed applicant for MIPLATFORM MEDICAL IMAGING SUITE?

The FDA 510(k) record lists Hinacom Software and Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIPLATFORM MEDICAL IMAGING SUITE?

The FDA product code for MIPLATFORM MEDICAL IMAGING SUITE 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 Hinacom Software and Technology, Ltd. 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.

K171977miPlatform medical imaging suite v3.0 (miPlatform v3.0), miPlatform ZFP Viewer

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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