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FDA 510(k)

MODEL FORTY ULTRA COMPACT VIDEO IMAGER

K-Number: K940332 · 1994-06-08

ApplicantInternational Imaging Electronics
Decision Date1994-06-08
Product CodeLMC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL FORTY ULTRA COMPACT VIDEO IMAGER 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 1994-06-08 under 510(k) number K940332. 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 MODEL FORTY ULTRA COMPACT VIDEO IMAGER?

MODEL FORTY ULTRA COMPACT VIDEO IMAGER is a medical device that received FDA 510(k) clearance on 1994-06-08. The listed applicant is International Imaging Electronics. The 510(k) number is K940332.

When did MODEL FORTY ULTRA COMPACT VIDEO IMAGER receive FDA 510(k) clearance?

MODEL FORTY ULTRA COMPACT VIDEO IMAGER received FDA 510(k) clearance on 1994-06-08, under 510(k) number K940332.

Who is the listed applicant for MODEL FORTY ULTRA COMPACT VIDEO IMAGER?

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 MODEL FORTY ULTRA COMPACT VIDEO IMAGER?

The FDA product code for MODEL FORTY ULTRA COMPACT VIDEO IMAGER 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 IMAGERK934908FULL VIEW DIGITAL STORAGE SYSTEMK930755ULTRA COMPACT VIDEO IMAGER

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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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