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FDA 510(k)

CHASE CARDIAC ANALYSIS SYSTEM

K-Number: K062031 · 2006-09-27

ApplicantChase Medical, LP
Decision Date2006-09-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CHASE CARDIAC ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Chase Medical, LP. It received FDA 510(k) clearance on 2006-09-27 under 510(k) number K062031. 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 CHASE CARDIAC ANALYSIS SYSTEM?

CHASE CARDIAC ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 2006-09-27. The listed applicant is Chase Medical, LP. The 510(k) number is K062031.

When did CHASE CARDIAC ANALYSIS SYSTEM receive FDA 510(k) clearance?

CHASE CARDIAC ANALYSIS SYSTEM received FDA 510(k) clearance on 2006-09-27, under 510(k) number K062031.

Who is the listed applicant for CHASE CARDIAC ANALYSIS SYSTEM?

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

What is the FDA product code for CHASE CARDIAC ANALYSIS SYSTEM?

The FDA product code for CHASE CARDIAC ANALYSIS SYSTEM 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 Chase Medical, LP 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.

K072473CHASE MR SYSTEM

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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