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FDA 510(k)

MODEL 78670A

K-Number: K823268 · 1983-01-26

ApplicantHewlett-Packard Co.
Decision Date1983-01-26
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 78670A 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 1983-01-26 under 510(k) number K823268. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 78670A?

MODEL 78670A is a medical device that received FDA 510(k) clearance on 1983-01-26. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K823268.

When did MODEL 78670A receive FDA 510(k) clearance?

MODEL 78670A received FDA 510(k) clearance on 1983-01-26, under 510(k) number K823268.

Who is the listed applicant for MODEL 78670A?

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 78670A?

The FDA product code for MODEL 78670A is LDD.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: LDD)

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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