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FDA 510(k)

MODEL 15050A DIGITAL DISPLAY

K-Number: K761211 · 1976-12-13

ApplicantHewlett-Packard Co.
Decision Date1976-12-13
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 15050A DIGITAL 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 1976-12-13 under 510(k) number K761211. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 15050A DIGITAL DISPLAY?

MODEL 15050A DIGITAL DISPLAY is a medical device that received FDA 510(k) clearance on 1976-12-13. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K761211.

When did MODEL 15050A DIGITAL DISPLAY receive FDA 510(k) clearance?

MODEL 15050A DIGITAL DISPLAY received FDA 510(k) clearance on 1976-12-13, under 510(k) number K761211.

Who is the listed applicant for MODEL 15050A DIGITAL 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 MODEL 15050A DIGITAL DISPLAY?

The FDA product code for MODEL 15050A DIGITAL DISPLAY is DRT.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DRT)

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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