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FDA 510(k)

HP M1205A OMNICARE COMPONENT TRANSPORT MONITORING SYSTEM MODEL 24

K-Number: K950821 · 1995-10-03

Decision Date1995-10-03
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HP M1205A OMNICARE COMPONENT TRANSPORT MONITORING 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 1995-10-03 under 510(k) number K950821. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP M1205A OMNICARE COMPONENT TRANSPORT MONITORING SYSTEM MODEL 24?

HP M1205A OMNICARE COMPONENT TRANSPORT MONITORING SYSTEM MODEL 24 is a medical device that received FDA 510(k) clearance on 1995-10-03. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K950821.

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

HP M1205A OMNICARE COMPONENT TRANSPORT MONITORING SYSTEM MODEL 24 received FDA 510(k) clearance on 1995-10-03, under 510(k) number K950821.

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

The FDA product code for HP M1205A OMNICARE COMPONENT TRANSPORT MONITORING SYSTEM MODEL 24 is DSI.

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: DSI)

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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