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FDA 510(k)

MULTI FORMAT VIDEO IMAGER 600 PLUS

K-Number: K904363 · 1990-11-13

ApplicantInternational Imaging Electronics
Decision Date1990-11-13
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTI FORMAT VIDEO IMAGER 600 PLUS is the device name listed in this FDA 510(k) record. The listed applicant is International Imaging Electronics. It received FDA 510(k) clearance on 1990-11-13 under 510(k) number K904363. 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 MULTI FORMAT VIDEO IMAGER 600 PLUS?

MULTI FORMAT VIDEO IMAGER 600 PLUS is a medical device that received FDA 510(k) clearance on 1990-11-13. The listed applicant is International Imaging Electronics. The 510(k) number is K904363.

When did MULTI FORMAT VIDEO IMAGER 600 PLUS receive FDA 510(k) clearance?

MULTI FORMAT VIDEO IMAGER 600 PLUS received FDA 510(k) clearance on 1990-11-13, under 510(k) number K904363.

Who is the listed applicant for MULTI FORMAT VIDEO IMAGER 600 PLUS?

The FDA 510(k) record lists International Imaging Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI FORMAT VIDEO IMAGER 600 PLUS?

The FDA product code for MULTI FORMAT VIDEO IMAGER 600 PLUS is LMC.

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Other records listing International Imaging Electronics 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.

K972019PEFECT SHOTK970964MAESTRO DIGITAL IMAGE AND PATIENT RECORD STORAGE SYSTEMK950330DIGITAL IMAGE ACQUISITION SYSTEMK953165ULTRA COMPACT VIDEO IMAGERK940332MODEL FORTY ULTRA COMPACT VIDEO IMAGERK934908FULL VIEW DIGITAL STORAGE SYSTEM

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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

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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