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FDA 510(k)

GMC Wrist Automatic Blood Pressure Monitor

K-Number: K181930 · 2019-02-14

ApplicantGmc, Inc.
Decision Date2019-02-14
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GMC Wrist Automatic Blood Pressure Monitor is a medical device manufactured by Gmc, Inc.. It received FDA 510(k) clearance on 2019-02-14 under approval number K181930. 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 GMC Wrist Automatic Blood Pressure Monitor?

GMC Wrist Automatic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-02-14. It is manufactured by Gmc, Inc.. The 510(k) number is K181930.

When was GMC Wrist Automatic Blood Pressure Monitor approved by the FDA?

GMC Wrist Automatic Blood Pressure Monitor received FDA 510(k) clearance on 2019-02-14, under approval number K181930.

What company makes GMC Wrist Automatic Blood Pressure Monitor?

GMC Wrist Automatic Blood Pressure Monitor is manufactured by Gmc, Inc..

What is the FDA product code for GMC Wrist Automatic Blood Pressure Monitor?

The FDA product code for GMC Wrist Automatic Blood Pressure Monitor is DXN.

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Official Source

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