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FDA 510(k)

MODELS M1175A AND M1176A COMPONENT MONITORING SYST

K-Number: K922058 · 1992-10-06

Decision Date1992-10-06
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS M1175A AND M1176A COMPONENT MONITORING SYST 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 1992-10-06 under 510(k) number K922058. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS M1175A AND M1176A COMPONENT MONITORING SYST?

MODELS M1175A AND M1176A COMPONENT MONITORING SYST is a medical device that received FDA 510(k) clearance on 1992-10-06. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K922058.

When did MODELS M1175A AND M1176A COMPONENT MONITORING SYST receive FDA 510(k) clearance?

MODELS M1175A AND M1176A COMPONENT MONITORING SYST received FDA 510(k) clearance on 1992-10-06, under 510(k) number K922058.

Who is the listed applicant for MODELS M1175A AND M1176A COMPONENT MONITORING SYST?

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 M1175A AND M1176A COMPONENT MONITORING SYST?

The FDA product code for MODELS M1175A AND M1176A COMPONENT MONITORING SYST is MHX.

Related Clinical Trials

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.

Other records listing Hewlett-Packard Co. as applicant

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.

View all 230 devices →

Related Devices (Code: MHX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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