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FDA 510(k)

MODELS 78551A 78552A

K-Number: K841256 · 1984-10-02

ApplicantHewlett-Packard Co.
Decision Date1984-10-02
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS 78551A 78552A 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 1984-10-02 under 510(k) number K841256. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS 78551A 78552A?

MODELS 78551A 78552A is a medical device that received FDA 510(k) clearance on 1984-10-02. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K841256.

When did MODELS 78551A 78552A receive FDA 510(k) clearance?

MODELS 78551A 78552A received FDA 510(k) clearance on 1984-10-02, under 510(k) number K841256.

Who is the listed applicant for MODELS 78551A 78552A?

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 MODELS 78551A 78552A?

The FDA product code for MODELS 78551A 78552A is DXG.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DXG)

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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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