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FDA 510(k)

ANGIOTEC ZX DIGITAL IMAGE PROCESSOR

K-Number: K892869 · 1989-05-26

ApplicantAndros Analyzers, Inc.
Decision Date1989-05-26
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ANGIOTEC ZX DIGITAL IMAGE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Andros Analyzers, Inc.. It received FDA 510(k) clearance on 1989-05-26 under 510(k) number K892869. 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 ANGIOTEC ZX DIGITAL IMAGE PROCESSOR?

ANGIOTEC ZX DIGITAL IMAGE PROCESSOR is a medical device that received FDA 510(k) clearance on 1989-05-26. The listed applicant is Andros Analyzers, Inc.. The 510(k) number is K892869.

When did ANGIOTEC ZX DIGITAL IMAGE PROCESSOR receive FDA 510(k) clearance?

ANGIOTEC ZX DIGITAL IMAGE PROCESSOR received FDA 510(k) clearance on 1989-05-26, under 510(k) number K892869.

Who is the listed applicant for ANGIOTEC ZX DIGITAL IMAGE PROCESSOR?

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

What is the FDA product code for ANGIOTEC ZX DIGITAL IMAGE PROCESSOR?

The FDA product code for ANGIOTEC ZX DIGITAL IMAGE PROCESSOR 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 Andros Analyzers, 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.

K903806ANGIOTEC IMAGE MANAGEMENT SYSTEMK893476ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV.K891485ANGIOTEC FMX-2220 SYSTEMK852463ANDROS ANALYZERS AIRWAY ADAPTER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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