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FDA 510(k)

MODEL 5621A INTERFACE

K-Number: K780768 · 1978-05-26

ApplicantHewlett-Packard Co.
Decision Date1978-05-26
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 5621A INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1978-05-26 under 510(k) number K780768. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 5621A INTERFACE?

MODEL 5621A INTERFACE is a medical device that received FDA 510(k) clearance on 1978-05-26. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K780768.

When did MODEL 5621A INTERFACE receive FDA 510(k) clearance?

MODEL 5621A INTERFACE received FDA 510(k) clearance on 1978-05-26, under 510(k) number K780768.

Who is the listed applicant for MODEL 5621A INTERFACE?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 5621A INTERFACE?

The FDA product code for MODEL 5621A INTERFACE is DQK.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DQK)

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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