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FDA 510(k)

PMP4 BP PRO BLOOD PRESSURE MONITOR

K-Number: K060703 · 2006-04-04

Decision Date2006-04-04
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PMP4 BP PRO BLOOD PRESSURE MONITOR 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 2006-04-04 under 510(k) number K060703. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMP4 BP PRO BLOOD PRESSURE MONITOR?

PMP4 BP PRO BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 2006-04-04. The listed applicant is Card Guard Scientific Survival , Ltd.. The 510(k) number is K060703.

When did PMP4 BP PRO BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

PMP4 BP PRO BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 2006-04-04, under 510(k) number K060703.

Who is the listed applicant for PMP4 BP PRO BLOOD PRESSURE MONITOR?

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 BP PRO BLOOD PRESSURE MONITOR?

The FDA product code for PMP4 BP PRO BLOOD PRESSURE MONITOR is DXN.

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 Card Guard Scientific Survival , Ltd. 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 49 devices →

Related Devices (Code: DXN)

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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