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FDA 510(k)

SAECG CARDIOGRAPH MODEL M1754A

K-Number: K913997 · 1992-03-06

ApplicantHewlett-Packard Co.
Decision Date1992-03-06
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SAECG CARDIOGRAPH MODEL M1754A 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 1992-03-06 under 510(k) number K913997. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAECG CARDIOGRAPH MODEL M1754A?

SAECG CARDIOGRAPH MODEL M1754A is a medical device that received FDA 510(k) clearance on 1992-03-06. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K913997.

When did SAECG CARDIOGRAPH MODEL M1754A receive FDA 510(k) clearance?

SAECG CARDIOGRAPH MODEL M1754A received FDA 510(k) clearance on 1992-03-06, under 510(k) number K913997.

Who is the listed applicant for SAECG CARDIOGRAPH MODEL M1754A?

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 SAECG CARDIOGRAPH MODEL M1754A?

The FDA product code for SAECG CARDIOGRAPH MODEL M1754A is KNT.

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Related Devices (Code: KNT)

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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