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FDA 510(k)

HEM-6410T-ZM Wrist Blood Pressure Monitor

K-Number: K182481 · 2018-11-09

Decision Date2018-11-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEM-6410T-ZM Wrist Blood Pressure Monitor is a medical device manufactured by Omron Healthcare, Inc.. It received FDA 510(k) clearance on 2018-11-09 under approval number K182481. 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 HEM-6410T-ZM Wrist Blood Pressure Monitor?

HEM-6410T-ZM Wrist Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2018-11-09. It is manufactured by Omron Healthcare, Inc.. The 510(k) number is K182481.

When was HEM-6410T-ZM Wrist Blood Pressure Monitor approved by the FDA?

HEM-6410T-ZM Wrist Blood Pressure Monitor received FDA 510(k) clearance on 2018-11-09, under approval number K182481.

What company makes HEM-6410T-ZM Wrist Blood Pressure Monitor?

HEM-6410T-ZM Wrist Blood Pressure Monitor is manufactured by Omron Healthcare, Inc..

What is the FDA product code for HEM-6410T-ZM Wrist Blood Pressure Monitor?

The FDA product code for HEM-6410T-ZM Wrist Blood Pressure Monitor is DXN.

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Official Source

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