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FDA 510(k)

MODELS 78504A & 78508A PATIENT MON. SYS

K-Number: K821368 · 1982-05-25

ApplicantHewlett-Packard Co.
Decision Date1982-05-25
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS 78504A & 78508A PATIENT MON. SYS 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 1982-05-25 under 510(k) number K821368. 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 MODELS 78504A & 78508A PATIENT MON. SYS?

MODELS 78504A & 78508A PATIENT MON. SYS is a medical device that received FDA 510(k) clearance on 1982-05-25. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K821368.

When did MODELS 78504A & 78508A PATIENT MON. SYS receive FDA 510(k) clearance?

MODELS 78504A & 78508A PATIENT MON. SYS received FDA 510(k) clearance on 1982-05-25, under 510(k) number K821368.

Who is the listed applicant for MODELS 78504A & 78508A PATIENT MON. SYS?

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 78504A & 78508A PATIENT MON. SYS?

The FDA product code for MODELS 78504A & 78508A PATIENT MON. SYS 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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