FDA 510(k)

HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE

K-Number: K942842 · 1995-02-16

Decision Date1995-02-16

Product CodeDQA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard GmbH. It received FDA 510(k) clearance on 1995-02-16 under 510(k) number K942842. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE?

HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE is a medical device that received FDA 510(k) clearance on 1995-02-16. The listed applicant is Hewlett-Packard GmbH. The 510(k) number is K942842.

When did HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE receive FDA 510(k) clearance?

HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE received FDA 510(k) clearance on 1995-02-16, under 510(k) number K942842.

Who is the listed applicant for HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE?

The FDA 510(k) record lists Hewlett-Packard GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE?

The FDA product code for HEWLETT-PACKARD M1021A MIX VEN OXY SAT PLUG-IN MODULE is DQA.

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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.