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FDA 510(k)

DIGITAL IMAGE ACQUISITION SYSTEM

K-Number: K950330 · 1996-05-07

ApplicantInternational Imaging Electronics
Decision Date1996-05-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL IMAGE ACQUISITION SYSTEM 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 1996-05-07 under 510(k) number K950330. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL IMAGE ACQUISITION SYSTEM?

DIGITAL IMAGE ACQUISITION SYSTEM is a medical device that received FDA 510(k) clearance on 1996-05-07. The listed applicant is International Imaging Electronics. The 510(k) number is K950330.

When did DIGITAL IMAGE ACQUISITION SYSTEM receive FDA 510(k) clearance?

DIGITAL IMAGE ACQUISITION SYSTEM received FDA 510(k) clearance on 1996-05-07, under 510(k) number K950330.

Who is the listed applicant for DIGITAL IMAGE ACQUISITION SYSTEM?

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 DIGITAL IMAGE ACQUISITION SYSTEM?

The FDA product code for DIGITAL IMAGE ACQUISITION SYSTEM is IYO.

Related Clinical Trials

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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 SYSTEMK953165ULTRA COMPACT VIDEO IMAGERK940332MODEL FORTY ULTRA COMPACT VIDEO IMAGERK934908FULL VIEW DIGITAL STORAGE SYSTEMK930755ULTRA COMPACT VIDEO IMAGER

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Related Devices (Code: IYO)

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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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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