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FDA 510(k)

AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE

K-Number: K102534 · 2011-05-24

ApplicantAze, Ltd.
Decision Date2011-05-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Aze, Ltd.. It received FDA 510(k) clearance on 2011-05-24 under 510(k) number K102534. 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 AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE?

AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE is a medical device that received FDA 510(k) clearance on 2011-05-24. The listed applicant is Aze, Ltd.. The 510(k) number is K102534.

When did AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE receive FDA 510(k) clearance?

AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE received FDA 510(k) clearance on 2011-05-24, under 510(k) number K102534.

Who is the listed applicant for AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE?

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

What is the FDA product code for AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE?

The FDA product code for AZE VIRTUALPLACE-MR FLOW ANALYSIS SOFTWARE 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 Aze, 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.

K060453AZE VIRTUALPLACE

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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