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FDA 510(k)

ECG SCOPE MODEL 7833

K-Number: K771360 · 1977-08-04

ApplicantHewlett-Packard Co.
Decision Date1977-08-04
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ECG SCOPE MODEL 7833 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 1977-08-04 under 510(k) number K771360. 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 ECG SCOPE MODEL 7833?

ECG SCOPE MODEL 7833 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K771360.

When did ECG SCOPE MODEL 7833 receive FDA 510(k) clearance?

ECG SCOPE MODEL 7833 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771360.

Who is the listed applicant for ECG SCOPE MODEL 7833?

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 ECG SCOPE MODEL 7833?

The FDA product code for ECG SCOPE MODEL 7833 is DRT.

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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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