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FDA 510(k)

COR ANALYZER II, MODEL V1.7

K-Number: K072242 · 2007-09-11

ApplicantRcadia Medical Imaging , Ltd.
Decision Date2007-09-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COR ANALYZER II, MODEL V1.7 is the device name listed in this FDA 510(k) record. The listed applicant is Rcadia Medical Imaging , Ltd.. It received FDA 510(k) clearance on 2007-09-11 under 510(k) number K072242. 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 COR ANALYZER II, MODEL V1.7?

COR ANALYZER II, MODEL V1.7 is a medical device that received FDA 510(k) clearance on 2007-09-11. The listed applicant is Rcadia Medical Imaging , Ltd.. The 510(k) number is K072242.

When did COR ANALYZER II, MODEL V1.7 receive FDA 510(k) clearance?

COR ANALYZER II, MODEL V1.7 received FDA 510(k) clearance on 2007-09-11, under 510(k) number K072242.

Who is the listed applicant for COR ANALYZER II, MODEL V1.7?

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

What is the FDA product code for COR ANALYZER II, MODEL V1.7?

The FDA product code for COR ANALYZER II, MODEL V1.7 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 Rcadia Medical Imaging , 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.

K110071COR ANALYZERK063548COR ANALYZER 1, VERSION 1.4

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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