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FDA 510(k)

MODEL 80100A, PATIENT DATA MEMORY

K-Number: K781360 · 1978-09-07

ApplicantHewlett-Packard Co.
Decision Date1978-09-07
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL 80100A, PATIENT DATA MEMORY 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 1978-09-07 under 510(k) number K781360. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 80100A, PATIENT DATA MEMORY?

MODEL 80100A, PATIENT DATA MEMORY is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K781360.

When did MODEL 80100A, PATIENT DATA MEMORY receive FDA 510(k) clearance?

MODEL 80100A, PATIENT DATA MEMORY received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781360.

Who is the listed applicant for MODEL 80100A, PATIENT DATA MEMORY?

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 80100A, PATIENT DATA MEMORY?

The FDA product code for MODEL 80100A, PATIENT DATA MEMORY is HGM.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: HGM)

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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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