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FDA 510(k)

PATIENT MONITORS MODELS 78701A/78702A

K-Number: K771572 · 1977-08-30

ApplicantHewlett-Packard Co.
Decision Date1977-08-30
Product CodeDRR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITORS MODELS 78701A/78702A 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 1977-08-30 under 510(k) number K771572. The device is classified under product code DRR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITORS MODELS 78701A/78702A?

PATIENT MONITORS MODELS 78701A/78702A is a medical device that received FDA 510(k) clearance on 1977-08-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K771572.

When did PATIENT MONITORS MODELS 78701A/78702A receive FDA 510(k) clearance?

PATIENT MONITORS MODELS 78701A/78702A received FDA 510(k) clearance on 1977-08-30, under 510(k) number K771572.

Who is the listed applicant for PATIENT MONITORS MODELS 78701A/78702A?

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 PATIENT MONITORS MODELS 78701A/78702A?

The FDA product code for PATIENT MONITORS MODELS 78701A/78702A is DRR.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DRR)

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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