FDA 510(k)

MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P

K-Number: K120430 · 2012-08-02

ApplicantMicrolife Intellectual Property GmbH

Decision Date2012-08-02

Product CodeDXN

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2012-08-02 under 510(k) number K120430. 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 MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P?

MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P is a medical device that received FDA 510(k) clearance on 2012-08-02. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K120430.

When did MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P receive FDA 510(k) clearance?

MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P received FDA 510(k) clearance on 2012-08-02, under 510(k) number K120430.

Who is the listed applicant for MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P?

The FDA 510(k) record lists Microlife Intellectual Property GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P?

The FDA product code for MICROLIFE WRIST WATCH BLOOD PREEURE MONITOR, BP3MO1-3P is DXN.

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Related Devices (Code: DXN)

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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.