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FDA 510(k)

IMAGEVIEW 5000

K-Number: K925650 · 1993-09-14

ApplicantNuclear Data Systems
Decision Date1993-09-14
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMAGEVIEW 5000 is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Data Systems. It received FDA 510(k) clearance on 1993-09-14 under 510(k) number K925650. The device is classified under product code LMC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMAGEVIEW 5000?

IMAGEVIEW 5000 is a medical device that received FDA 510(k) clearance on 1993-09-14. The listed applicant is Nuclear Data Systems. The 510(k) number is K925650.

When did IMAGEVIEW 5000 receive FDA 510(k) clearance?

IMAGEVIEW 5000 received FDA 510(k) clearance on 1993-09-14, under 510(k) number K925650.

Who is the listed applicant for IMAGEVIEW 5000?

The FDA 510(k) record lists Nuclear Data Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMAGEVIEW 5000?

The FDA product code for IMAGEVIEW 5000 is LMC.

Related Clinical Trials

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Other records listing Nuclear Data Systems 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.

K896540ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE

Related Devices (Code: LMC)

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.

K111566DRYVIEW CHROMA IMAGING SYSTEMCarestream Health, Inc.K092280CYPHER DICOM PRINT SOLUTIONVirtual Imaging, Inc.K090469CARESTREAM DRYVIEW 5850 LASER IMAGERCarestream Health, Inc.K083522SONY UP-DF750 DIGITAL FILM IMAGERSony Electronics, Inc.K081637LASER IMAGER DRYPRO MODEL 873Konica Minolta Medical & Graphic, Inc.K072680DRYSTAR AXYS, MODEL EYZ4EAgfa Healthcare Corporation

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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