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FDA 510(k)

HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24

K-Number: K960934 · 1996-06-14

ApplicantHewlett-Packard Co.
Decision Date1996-06-14
Product CodeMLD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24 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 1996-06-14 under 510(k) number K960934. The device is classified under product code MLD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24?

HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24 is a medical device that received FDA 510(k) clearance on 1996-06-14. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K960934.

When did HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24 receive FDA 510(k) clearance?

HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24 received FDA 510(k) clearance on 1996-06-14, under 510(k) number K960934.

Who is the listed applicant for HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24?

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 HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24?

The FDA product code for HP M1205A OMNICARE COMPONENT MONITOR SYSTEM MODEL 24 is MLD.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: MLD)

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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