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FDA 510(k)

DIGITAL IMAGE MEMORY/PROCESSOR

K-Number: K781056 · 1978-08-14

ApplicantQuantex Corp.
Decision Date1978-08-14
Product Code
DecisionSubstantially Equivalent

Device Summary

DIGITAL IMAGE MEMORY/PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Quantex Corp.. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K781056. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL IMAGE MEMORY/PROCESSOR?

DIGITAL IMAGE MEMORY/PROCESSOR is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Quantex Corp.. The 510(k) number is K781056.

When did DIGITAL IMAGE MEMORY/PROCESSOR receive FDA 510(k) clearance?

DIGITAL IMAGE MEMORY/PROCESSOR received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781056.

Who is the listed applicant for DIGITAL IMAGE MEMORY/PROCESSOR?

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

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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

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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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