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FDA 510(k)

M. 1336S CATHODE-RAY TUBE DISPLAY

K-Number: K780782 · 1978-06-14

ApplicantHewlett-Packard Co.
Decision Date1978-06-14
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M. 1336S CATHODE-RAY TUBE DISPLAY 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 1978-06-14 under 510(k) number K780782. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M. 1336S CATHODE-RAY TUBE DISPLAY?

M. 1336S CATHODE-RAY TUBE DISPLAY is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K780782.

When did M. 1336S CATHODE-RAY TUBE DISPLAY receive FDA 510(k) clearance?

M. 1336S CATHODE-RAY TUBE DISPLAY received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780782.

Who is the listed applicant for M. 1336S CATHODE-RAY TUBE DISPLAY?

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 M. 1336S CATHODE-RAY TUBE DISPLAY?

The FDA product code for M. 1336S CATHODE-RAY TUBE DISPLAY is DXJ.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DXJ)

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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