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FDA 510(k)

HP MODEL 8880A FILTER

K-Number: K802686 · 1980-11-26

ApplicantHewlett-Packard Co.
Decision Date1980-11-26
Product CodeDRR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HP MODEL 8880A FILTER 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 1980-11-26 under 510(k) number K802686. The device is classified under product code DRR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP MODEL 8880A FILTER?

HP MODEL 8880A FILTER is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K802686.

When did HP MODEL 8880A FILTER receive FDA 510(k) clearance?

HP MODEL 8880A FILTER received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802686.

Who is the listed applicant for HP MODEL 8880A FILTER?

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 HP MODEL 8880A FILTER?

The FDA product code for HP MODEL 8880A FILTER is DRR.

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Other records listing Hewlett-Packard Co. 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.

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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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