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FDA 510(k)

MONITOR SCOPE

K-Number: K760523 · 1976-09-03

ApplicantHewlett-Packard Co.
Decision Date1976-09-03
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITOR SCOPE 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 1976-09-03 under 510(k) number K760523. 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 MONITOR SCOPE?

MONITOR SCOPE is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K760523.

When did MONITOR SCOPE receive FDA 510(k) clearance?

MONITOR SCOPE received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760523.

Who is the listed applicant for MONITOR SCOPE?

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 MONITOR SCOPE?

The FDA product code for MONITOR SCOPE 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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