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FDA 510(k)

PMP4 OXY PRO

K-Number: K043162 · 2004-12-29

ApplicantCard Guard Scientific Survival , Ltd.
Decision Date2004-12-29
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PMP4 OXY PRO is the device name listed in this FDA 510(k) record. The listed applicant is Card Guard Scientific Survival , Ltd.. It received FDA 510(k) clearance on 2004-12-29 under 510(k) number K043162. 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 PMP4 OXY PRO?

PMP4 OXY PRO is a medical device that received FDA 510(k) clearance on 2004-12-29. The listed applicant is Card Guard Scientific Survival , Ltd.. The 510(k) number is K043162.

When did PMP4 OXY PRO receive FDA 510(k) clearance?

PMP4 OXY PRO received FDA 510(k) clearance on 2004-12-29, under 510(k) number K043162.

Who is the listed applicant for PMP4 OXY PRO?

The FDA 510(k) record lists Card Guard Scientific Survival , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PMP4 OXY PRO?

The FDA product code for PMP4 OXY PRO is DQA.

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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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